Product Details

SNP ID

rs2662959

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:10680272 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCCCGCTGGAGCCTGTGGGTCTCTT[C/T]CCTGAGAACTGTGTGCAGCCATCTA

Phenotype

MIM: 160720 MIM: 603644

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYH3 PubMed Links

Gene Details

Gene

MYH3

Gene Name

myosin, heavy chain 3, skeletal muscle, embryonic

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002470.3	1781	Intron			NP_002461.2
XM_011523870.2	1781	Intron			XP_011522172.1
XM_011523871.2	1781	Intron			XP_011522173.1

Gene

SCO1

Gene Name

SCO1 cytochrome c oxidase assembly protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004589.3	1781	Intron			NP_004580.1
XM_005256751.3	1781	UTR 3			XP_005256808.1

View Full Product Details