ClinVar

NM_000260.4(MYO7A):c.3862G>C (p.Ala1288Pro)

Gene:

MYO7A:myosin VIIA [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.5

Genomic location:

• Chr11: 77190808 (on Assembly GRCh38)
• Chr11: 76901853 (on Assembly GRCh37)

Preferred name:

NM_000260.4(MYO7A):c.3862G>C (p.Ala1288Pro)

Other names:

NM_000260.4(MYO7A):c.3862G>C; p.Ala1288Pro

HGVS:

• NC_000011.10:g.77190808G>C
• NG_009086.2:g.67563G>C
• NM_000260.4:c.3862G>CMANE SELECT
• NM_001127180.2:c.3862G>C
• NM_001369365.1:c.3829G>C
• NP_000251.3:p.Ala1288Pro
• NP_001120652.1:p.Ala1288Pro
• NP_001356294.1:p.Ala1277Pro
• LRG_1420t1:c.3862G>C
• LRG_1420:g.67563G>C
• LRG_1420p1:p.Ala1288Pro
• NC_000011.9:g.76901853G>C
• NG_009086.1:g.67544G>C
• NM_000260.3:c.3862G>C

This HGVS expression did not pass validation

Protein change:

A1277P

Links:

dbSNP: rs749747871

NCBI 1000 Genomes Browser:

rs749747871

Molecular consequence:

• NM_000260.4:c.3862G>C - missense variant - [Sequence Ontology: SO:0001583]
• NM_001127180.2:c.3862G>C - missense variant - [Sequence Ontology: SO:0001583]
• NM_001369365.1:c.3829G>C - missense variant - [Sequence Ontology: SO:0001583]