Product Details

SNP ID

rs201502354

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:44964086 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACGGCCCGCATCACCCGGTACTGC[C/T]GGTCAGGGTCCAGCTTGTAGAGGTG

Phenotype

MIM: 600642

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYO1G PubMed Links

Gene Details

Gene

MYO1G

Gene Name

myosin IG

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033054.2	2611	Missense Mutation	CAG,CGG	Q903R	NP_149043.2
XM_017012503.1	2611	Missense Mutation	CAG,CGG	Q788R	XP_016867992.1
XM_017012504.1	2611	Missense Mutation	CAG,CGG	Q665R	XP_016867993.1

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