ClinVar

NM_000260.4(MYO7A):c.2076G>A (p.Val692=)

Gene:

MYO7A:myosin VIIA [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.5

Genomic location:

• Chr11: 77174896 (on Assembly GRCh38)
• Chr11: 76885942 (on Assembly GRCh37)

Preferred name:

NM_000260.4(MYO7A):c.2076G>A (p.Val692=)

HGVS:

• NC_000011.10:g.77174896G>A
• NG_009086.2:g.51651G>A
• NM_000260.4:c.2076G>AMANE SELECT
• NM_001127180.2:c.2076G>A
• NM_001369365.1:c.2043G>A
• NP_000251.3:p.Val692=
• NP_001120652.1:p.Val692=
• NP_001356294.1:p.Val681=
• LRG_1420t1:c.2076G>A
• LRG_1420:g.51651G>A
• LRG_1420p1:p.Val692=
• NC_000011.9:g.76885942G>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_000260.4:c.2076G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001127180.2:c.2076G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001369365.1:c.2043G>A - synonymous variant - [Sequence Ontology: SO:0001819]