Product Details

SNP ID

rs2240389

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:101613553 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGTTGCCGCACACATCTGGGGGAAA[C/T]GCTGCAAACATCTGCTTGACCTGAG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYL10 PubMed Links

Gene Details

Gene

MYL10

Gene Name

myosin light chain 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138403.4	501	Silent Mutation	GCA,GCG	A201A	NP_612412.2
XM_017012793.1	501	Silent Mutation	GCA,GCG	A122A	XP_016868282.1

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