ClinVar

NM_198219.3(ING1):c.453G>A (p.Arg151=)

Gene:

ING1:inhibitor of growth family member 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

13q34

Genomic location:

• Chr13: 110719545 (on Assembly GRCh38)
• Chr13: 111371892 (on Assembly GRCh37)

Preferred name:

NM_198219.3(ING1):c.453G>A (p.Arg151=)

HGVS:

• NC_000013.11:g.110719545G>A
• NG_012197.1:g.11810G>A
• NM_001267728.1:c.402G>A
• NM_005537.5:c.882G>A
• NM_198217.3:c.321G>A
• NM_198218.3:c.246G>A
• NM_198219.3:c.453G>AMANE SELECT
• NP_001254657.1:p.Arg134=
• NP_005528.4:p.Arg294=
• NP_937860.1:p.Arg107=
• NP_937861.1:p.Arg82=
• NP_937862.1:p.Arg151=
• NC_000013.10:g.111371892G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs148838936

NCBI 1000 Genomes Browser:

rs148838936

Molecular consequence:

• NM_001267728.1:c.402G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_005537.5:c.882G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_198217.3:c.321G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_198218.3:c.246G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_198219.3:c.453G>A - synonymous variant - [Sequence Ontology: SO:0001819]