ClinVar

NM_000546.6(TP53):c.91G>A (p.Val31Ile)

Gene:

TP53:tumor protein p53 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17p13.1

Genomic location:

• Chr17: 7676387 (on Assembly GRCh38)
• Chr17: 7579705 (on Assembly GRCh37)

Preferred name:

NM_000546.6(TP53):c.91G>A (p.Val31Ile)

Other names:

p.V31I:GTT>ATT

HGVS:

• NC_000017.11:g.7676387C>T
• NG_017013.2:g.16164G>A
• NM_000546.6:c.91G>AMANE SELECT
• NM_001126112.3:c.91G>A
• NM_001126113.3:c.91G>A
• NM_001126114.3:c.91G>A
• NM_001126118.2:c.-27G>A
• NM_001276695.3:c.-27G>A
• NM_001276696.3:c.-27G>A
• NM_001276760.3:c.-27G>A
• NM_001276761.3:c.-27G>A
• NP_000537.3:p.Val31Ile
• NP_000537.3:p.Val31Ile
• NP_001119584.1:p.Val31Ile
• NP_001119585.1:p.Val31Ile
• NP_001119586.1:p.Val31Ile
• LRG_321t1:c.91G>A
• LRG_321:g.16164G>A
• LRG_321p1:p.Val31Ile
• NC_000017.10:g.7579705C>T
• NM_000546.4:c.91G>A
• NM_000546.5:c.91G>A
• P04637:p.Val31Ile
• p.V31I

This HGVS expression did not pass validation

Protein change:

V31I

Links:

UniProtKB: P04637#VAR_044554; dbSNP: rs201753350

NCBI 1000 Genomes Browser:

rs201753350

Molecular consequence:

• NM_001126118.2:c.-27G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001276695.3:c.-27G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001276696.3:c.-27G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001276760.3:c.-27G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001276761.3:c.-27G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_000546.6:c.91G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001126112.3:c.91G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001126113.3:c.91G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001126114.3:c.91G>A - missense variant - [Sequence Ontology: SO:0001583]