ClinVar

NM_000260.4(MYO7A):c.3660G>A (p.Pro1220=)

Gene:

MYO7A:myosin VIIA [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.5

Genomic location:

• Chr11: 77190049 (on Assembly GRCh38)
• Chr11: 76901094 (on Assembly GRCh37)

Preferred name:

NM_000260.4(MYO7A):c.3660G>A (p.Pro1220=)

HGVS:

• NC_000011.10:g.77190049G>A
• NG_009086.2:g.66804G>A
• NM_000260.4:c.3660G>AMANE SELECT
• NM_001127180.2:c.3660G>A
• NM_001369365.1:c.3627G>A
• NP_000251.3:p.Pro1220=
• NP_001120652.1:p.Pro1220=
• NP_001356294.1:p.Pro1209=
• LRG_1420t1:c.3660G>A
• LRG_1420:g.66804G>A
• LRG_1420p1:p.Pro1220=
• NC_000011.9:g.76901094G>A
• NG_009086.1:g.66785G>A
• NM_000260.3:c.3660G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs751497005

NCBI 1000 Genomes Browser:

rs751497005

Molecular consequence:

• NM_000260.4:c.3660G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001127180.2:c.3660G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001369365.1:c.3627G>A - synonymous variant - [Sequence Ontology: SO:0001819]