ClinVar

NM_000260.4(MYO7A):c.4130T>C (p.Phe1377Ser)

Gene:

MYO7A:myosin VIIA [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.5

Genomic location:

• Chr11: 77192256 (on Assembly GRCh38)
• Chr11: 76903301 (on Assembly GRCh37)

Preferred name:

NM_000260.4(MYO7A):c.4130T>C (p.Phe1377Ser)

HGVS:

• NC_000011.10:g.77192256T>C
• NG_009086.2:g.69011T>C
• NM_000260.4:c.4130T>CMANE SELECT
• NM_001127180.2:c.4130T>C
• NM_001369365.1:c.4097T>C
• NP_000251.3:p.Phe1377Ser
• NP_001120652.1:p.Phe1377Ser
• NP_001356294.1:p.Phe1366Ser
• LRG_1420t1:c.4130T>C
• LRG_1420:g.69011T>C
• LRG_1420p1:p.Phe1377Ser
• NC_000011.9:g.76903301T>C
• NG_009086.1:g.68992T>C

This HGVS expression did not pass validation

Protein change:

F1366S

Links:

dbSNP: rs777168937

NCBI 1000 Genomes Browser:

rs777168937

Molecular consequence:

• NM_000260.4:c.4130T>C - missense variant - [Sequence Ontology: SO:0001583]
• NM_001127180.2:c.4130T>C - missense variant - [Sequence Ontology: SO:0001583]
• NM_001369365.1:c.4097T>C - missense variant - [Sequence Ontology: SO:0001583]