ClinVar

NM_175914.5(HNF4A):c.*906A>C

Gene:

HNF4A:hepatocyte nuclear factor 4 alpha [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

20q13.12

Genomic location:

• Chr20: 44430571 (on Assembly GRCh38)
• Chr20: 43059211 (on Assembly GRCh37)

Preferred name:

NM_175914.5(HNF4A):c.*906A>C

HGVS:

• NC_000020.11:g.44430571A>C
• NG_009818.1:g.79771A>C
• NM_000457.6:c.*906A>C
• NM_001030003.3:c.*906A>C
• NM_001258355.2:c.*906A>C
• NM_001287182.2:c.*906A>C
• NM_001287183.2:c.*906A>C
• NM_175914.5:c.*906A>CMANE SELECT
• NM_178849.3:c.*906A>C
• LRG_483t2:c.*906A>C
• LRG_483:g.79771A>C
• NC_000020.10:g.43059211A>C
• NM_000457.4:c.*906A>C

This HGVS expression did not pass validation

Links:

dbSNP: rs3212210

NCBI 1000 Genomes Browser:

rs3212210

Molecular consequence:

• NM_000457.6:c.*906A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001030003.3:c.*906A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001258355.2:c.*906A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001287182.2:c.*906A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001287183.2:c.*906A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_175914.5:c.*906A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_178849.3:c.*906A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]