ClinVar

NM_000257.4(MYH7):c.4974C>T (p.Asp1658=)

Genes:

LOC126861897:BRD4-independent group 4 enhancer GRCh37_chr14:23884455-23885654 [Gene]
MYH7:myosin heavy chain 7 [Gene - OMIM - HGNC]
MHRT:myosin heavy chain associated RNA transcript [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

14q11.2

Genomic location:

• Chr14: 23415812 (on Assembly GRCh38)
• Chr14: 23885021 (on Assembly GRCh37)

Preferred name:

NM_000257.4(MYH7):c.4974C>T (p.Asp1658=)

Other names:

NM_000257.3(MYH7):c.4974C>T

HGVS:

• NC_000014.9:g.23415812G>A
• NG_007884.1:g.24850C>T
• NM_000257.4:c.4974C>TMANE SELECT
• NP_000248.2:p.Asp1658=
• LRG_384t1:c.4974C>T
• LRG_384:g.24850C>T
• NC_000014.8:g.23885021G>A
• NM_000257.2:c.4974C>T
• NM_000257.3:c.4974C>T
• NR_126491.1:n.244G>A
• c.4974C>T
• p.Asp1658Asp

This HGVS expression did not pass validation

Links:

dbSNP: rs374289523

NCBI 1000 Genomes Browser:

rs374289523

Molecular consequence:

• NR_126491.1:n.244G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_000257.4:c.4974C>T - synonymous variant - [Sequence Ontology: SO:0001819]