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 computed assertion could be determined for this classification!

Variant: NM_001754.5(RUNX1):c.1086G>T (p.Ser362=)

CA10014208

1078219 (ClinVar)

Gene: RUNX1
Condition: hereditary thrombocytopenia and hematologic cancer predisposition syndrome
Inheritance Mode: Autosomal dominant inheritance
Link to MONDO
UUID: 7f409c13-8f7f-4bd1-a46f-2a06bc3ceced
Approved on: 2022-07-05
Published on: 2022-07-05

HGVS expressions

NM_001754.5:c.1086G>T
NM_001754.5(RUNX1):c.1086G>T (p.Ser362=)
NC_000021.9:g.34792492C>A
CM000683.2:g.34792492C>A
NC_000021.8:g.36164789C>A
CM000683.1:g.36164789C>A
NC_000021.7:g.35086659C>A
NG_011402.2:g.1197220G>T
ENST00000675419.1:c.1086G>T
ENST00000300305.7:c.1086G>T
ENST00000344691.8:c.1005G>T
ENST00000399240.5:c.813G>T
ENST00000437180.5:c.1086G>T
ENST00000482318.5:c.*676G>T
NM_001001890.2:c.1005G>T
NM_001754.4:c.1086G>T
NM_001001890.3:c.1005G>T
More

Benign

Met criteria codes 3
BS1 BP4 BP7
Not Met criteria codes 23
BA1 PVS1 BS4 BS3 BS2 BP3 BP1 BP2 BP5 PS1 PS2 PS3 PS4 PP1 PP2 PP3 PP4 PM6 PM2 PM1 PM3 PM5 PM4

Evidence Links 0

Expert Panel

Criteria Specification Information

Criteria Specification: ClinGen Myeloid Malignancy Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 2

PDF
Criteria Specification Approval History
Criteria Specifications for this VCEP
Evidence submitted by expert panel
Myeloid Malignancy VCEP
NM_001754.5(RUNX1):c.1086G>T (p.Ser362=) is a synonymous variant. AF 0.0006271 (0.06271%)( 10/15946 in East Asian subpopulation in gnomAD v2.1.1.) is 0.015% between 0.15% (BS1). REVEL score not calculable as this is a synonymous variant. SpliceAI predicts the following: Acceptor loss 0.00, Donor loss 0.00, Acceptor gain 0.00, Donor gain 0.00 (BP4). Evolutionary conservation prediction algorithms predict the site as not being conserved (PhyloP score -0.503315 < 2.0 or the variant is the reference nucleotide in one primate and/or three mammal species) (BP7). In summary, this variant meets criteria to be classified as benign. ACMG/AMP criteria applied, as specified by the Myeloid Malignancy Variant Curation Expert Panel for RUNX1: BS1, BP4, BP7.
Met criteria codes
BS1
MAF 0.0006271 (0.06271%)( 10/15946 in East Asian subpopulation in gnomAD v2.1.1.) is 0.015% between 0.15%
BP4
REVEL score not calculable as this is a synonymous variant. SpliceAI predicts the following: Acceptor loss 0.00, Donor loss 0.00, Acceptor gain 0.00, Donor gain 0.00.
BP7
Evolutionary conservation prediction algorithms predict the site as not being conserved (PhyloP score -0.503315 < 2.0 or the variant is the reference nucleotide in one primate and/or three mammal species) (BP7).
Not Met criteria codes
BA1
MAF 0.0006271 (0.06271%)( 10/15946 in East Asian subpopulation in gnomAD v2.1.1.) is 0.015% between 0.15%
PVS1
Synonymous variant, not applicable.
BS4
No published literature is available on this variant
BS3
No published literature is available on this variant
BS2
This rule is not applicable for MM-VCEP
BP3
This rule is not applicable for MM-VCEP
BP1
This rule is not applicable for MM-VCEP
BP2
No published literature is available on this variant
BP5
This rule is not applicable for MM-VCEP
PS1
Synonymous variant, not applicable.
PS2
No published literature is available on this variant
PS3
No published literature is available on this variant
PS4
No published literature is available on this variant
PP1
No published literature is available on this variant
PP2
This rule is not applicable for MM-VCEP
PP3
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PP4
This rule is not applicable for MM-VCEP
PM6
No published literature is available on this variant
PM2
MAF 0.0006271 (0.06271%)( 10/15946 in East Asian subpopulation in gnomAD v2.1.1.) is 0.015% between 0.15%
PM1
This variant occurs outside of the established Runt homology domain (RHD)
PM3
This rule is not applicable for MM-VCEP
PM5
Synonymous variant, not applicable.
PM4
Synonymous variant
Curation History
The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. If you have questions about the information contained on this website, please see a health care professional.
¤ Powered by BCM's Genboree.