Evidence Repository
The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries. [Disclaimer]
  • Gene obtained from curated document aligns with the Allele Registry but not with ClinVar data
  • No CSPEC computer assertion could be determined for this classification!

Variant: NM_000546.5(TP53):c.993+1delG

CA645369685

428898 (ClinVar)

Gene: TP53
Condition: Li-Fraumeni syndrome
Inheritance Mode: Autosomal dominant inheritance
Link to MONDO
UUID: a608c703-2232-4c79-86dd-00844776434d
Approved on: 2024-08-05
Published on: 2024-08-05

HGVS expressions

NM_000546.5:c.993+1delG
NM_000546.5(TP53):c.993+1delG
NC_000017.11:g.7673535del
CM000679.2:g.7673535del
NC_000017.10:g.7576853del
CM000679.1:g.7576853del
NC_000017.9:g.7517578del
NG_017013.2:g.19017del
ENST00000503591.2:c.993+1del
ENST00000508793.6:c.993+1del
ENST00000509690.6:c.597+1del
ENST00000514944.6:c.714+1del
ENST00000604348.6:c.972+1del
ENST00000269305.9:c.993+1del
ENST00000269305.8:c.993+1del
ENST00000359597.8:c.993+1del
ENST00000413465.6:c.782+647del
ENST00000420246.6:c.993+1del
ENST00000445888.6:c.993+1del
ENST00000455263.6:c.993+1del
ENST00000504290.5:c.597+1del
ENST00000504937.5:c.597+1del
ENST00000510385.5:c.597+1del
ENST00000576024.1:c.53+1del
ENST00000610292.4:c.876+1del
ENST00000610538.4:c.876+1del
ENST00000610623.4:c.516+1del
ENST00000615910.4:c.960+1del
ENST00000617185.4:c.993+1del
ENST00000618944.4:c.516+1del
ENST00000619186.4:c.516+1del
ENST00000619485.4:c.876+1del
ENST00000620739.4:c.876+1del
ENST00000622645.4:c.876+1del
ENST00000635293.1:c.876+1del
NM_000546.5:c.993+1del
NM_001126112.2:c.993+1del
NM_001126113.2:c.993+1del
NM_001126114.2:c.993+1del
NM_001126115.1:c.597+1del
NM_001126116.1:c.597+1del
NM_001126117.1:c.597+1del
NM_001126118.1:c.876+1del
NM_001276695.1:c.876+1del
NM_001276696.1:c.876+1del
NM_001276697.1:c.516+1del
NM_001276698.1:c.516+1del
NM_001276699.1:c.516+1del
NM_001276760.1:c.876+1del
NM_001276761.1:c.876+1del
NM_001276695.2:c.876+1del
NM_001276696.2:c.876+1del
NM_001276697.2:c.516+1del
NM_001276698.2:c.516+1del
NM_001276699.2:c.516+1del
NM_001276760.2:c.876+1del
NM_001276761.2:c.876+1del
NM_000546.6:c.993+1del
NM_001126112.3:c.993+1del
NM_001126113.3:c.993+1del
NM_001126114.3:c.993+1del
NM_001126115.2:c.597+1del
NM_001126116.2:c.597+1del
NM_001126117.2:c.597+1del
NM_001126118.2:c.876+1del
NM_001276695.3:c.876+1del
NM_001276696.3:c.876+1del
NM_001276697.3:c.516+1del
NM_001276698.3:c.516+1del
NM_001276699.3:c.516+1del
NM_001276760.3:c.876+1del
NM_001276761.3:c.876+1del
More

Likely Pathogenic

Met criteria codes 4
PM2_Supporting PS4_Supporting PVS1_Strong PP1
Not Met criteria codes 20
BA1 PM5 PM3 PM1 PM4 PM6 BS2 BS3 BS4 BS1 BP2 BP3 BP4 BP5 BP7 PS1 PS3 PS2 PP4 PP3

Evidence Links 0

Expert Panel

Criteria Specification Information

Criteria Specification: ClinGen TP53 Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for TP53 Version 2.0.0

Criteria Specification Approval History
Criteria Specifications for this VCEP
Evidence submitted by expert panel
TP53 VCEP
The NM_000546.6:c.993+1del is a deletion of a single G nucleotide within the canonical donor site of exon 9 of TP53. Through exon 9 skipping, the variant is observed in an RT-PCR assay to produce multiple aberrant transcripts encoding frameshift alterations predicted to induce nonsense-mediated decay (PVS1(RNA); PMID: 10980596). This variant has been reported in 1 proband meeting Classic LFS criteria. Based on this evidence, this variant scores 1 total points meeting the TP53 VCEP phenotype scoring criteria of 1-1.5 points. (PS4_Supporting; PMID: 10980596). This variant has been reported to segregate with LFS-associated cancers in 3-4 meioses in 1 family (PP1; PMID: 10980596). This variant is absent from gnomAD v4.1.0 (PM2_Supporting).. In summary, this variant meets criteria to be classified as likely pathogenic for Li-Fraumeni syndrome based on the ACMG/AMP criteria applied, as specified by the TP53 Variant Curation Expert Panel: PVS1(RNA), PS4_Supporting, PP1, PM2_Supporting (Bayesian Points: 7; VCEP specifications version 2.0; 7/24/2024).
Met criteria codes
PM2_Supporting
This variant is absent from gnomAD v4.1.0 (PM2_Supporting).
PS4_Supporting
This variant has been reported in 1 proband meeting Classic LFS criteria. Based on this evidence, this variant scores 1 total points meeting the TP53 VCEP phenotype scoring criteria of 1-1.5 points. (PS4_Supporting; PMID: 10980596).
PVS1_Strong
The NM_000546.6:c.993+1del is a deletion of a single G nucleotide within the canonical donor site of exon 9 of TP53. Through exon 9 skipping, the variant is observed in an RT-PCR assay to produce multiple aberrant transcripts encoding frameshift alterations predicted to induce nonsense-mediated decay. Since the assay does not fully account for leakiness, code weight downgraded to Strong (PVS1_Strong (RNA); PMID: 10980596).
PP1
This variant has been reported to segregate with LFS-associated cancers in 3-4 meioses in 1 family (PP1; PMID: 10980596).
Not Met criteria codes
BA1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PM5
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PM3
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PM1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PM4
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PM6
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BS2
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BS3
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BS4
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BS1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BP2
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BP3
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BP4
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BP5
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
BP7
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PS1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PS3
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PS2
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PP4
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PP3
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
Curation History
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