Evidence Repository - Clinical Genome Resources

The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries. [Disclaimer]

Variant: NM_000545.6(HNF1A):c.1501+1G>A

Curation Version - 1.0
Curation History
JSON LD for Version 1.0

CA386970409

430837 (ClinVar)

Gene: HNF1A

Condition: monogenic diabetes

Inheritance Mode: Autosomal dominant inheritance

Link to MONDO

UUID: c5cc6716-ae85-43d2-855d-a1031a3b4091

Approved on: 2022-04-17

Published on: 2022-04-17

HGVS expressions

NM_000545.6:c.1501+1G>A

NM_000545.6(HNF1A):c.1501+1G>A

NC_000012.12:g.120997666G>A

CM000674.2:g.120997666G>A

NC_000012.11:g.121435469G>A

CM000674.1:g.121435469G>A

NC_000012.10:g.119919852G>A

NG_011731.2:g.23921G>A

ENST00000257555.11:c.1501+1G>A

ENST00000257555.10:c.1501+1G>A

ENST00000400024.6:c.1502G>A

ENST00000402929.5:n.2368G>A

ENST00000535955.5:n.218G>A

ENST00000538626.2:n.366G>A

ENST00000538646.5:c.*478G>A

ENST00000540108.1:c.*941+1G>A

ENST00000541395.5:c.1501+1G>A

ENST00000541924.5:c.*516G>A

ENST00000543255.1:n.546G>A

ENST00000543427.5:c.964+1G>A

ENST00000544413.2:c.1501+1G>A

ENST00000544574.5:c.*265G>A

ENST00000560968.5:n.1318+1G>A

ENST00000615446.4:c.289+1G>A

ENST00000617366.4:c.618+1G>A

NM_000545.5:c.1501+1G>A

NM_001306179.1:c.1501+1G>A

NM_000545.8:c.1501+1G>A

NM_001306179.2:c.1501+1G>A

NM_000545.8(HNF1A):c.1501+1G>A

Likely Pathogenic

The Expert Panel has overridden the computationally generated classification - "Uncertain Significance - Insufficient Evidence"

PVS1 PM2_Supporting

PS1

Evidence Links 0

Expert Panel

Monogenic Diabetes VCEP

Criteria Specification Information

Criteria Specifications for this VCEP

Evidence submitted by expert panel

Monogenic Diabetes VCEP

The c.1501+1G>A variant in the HNF1 homeobox A gene, HNF1A, is predicted to remove a canonical splice donor site in intron 7 of NM_000545.8. This variant is predicted to cause an in-frame deletion of biologically-relevant exon 7 of 10, removing more than 18% of the transactivation domain, a region important for protein function (PVS1; PMID: 23348805). Additionally, this variant is absent from gnomAD v2.1.1 (PM2_Supporting). The nucleotide change, c.1501+1G>T, which causes the same splice donor loss, has been reported in a patient with monogenic diabetes; however, the c.1501+1G>T variant has not met the criteria to be classified as pathogenic for monogenic diabetes by the ClinGen MDEP. In summary, c.1501+1G>A meets the criteria to be classified as likely pathogenic for monogenic diabetes. ACMG/AMP criteria applied, as specified by the ClinGen MDEP VCEP (specification version 1.1, approved 9/30/2021): PVS1, PM2_Supporting. 

PVS1

This variant is predicted to cause an in-frame deletion of biologically-relevant exon 7 of 10, removing more than 18% of the transactivation domain, a region important for protein function (PMID: 23348805).

PM2_Supporting

This variant is absent from gnomAD.

PS1

The nucleotide change, c.1501+1G>T, which causes the same splice donor loss, has been reported in a patient with monogenic diabetes; however, the c.1501+1G>T variant has not met the criteria to be classified as pathogenic for monogenic diabetes by the ClinGen MDEP.

Curation History

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