Product Details

SNP ID

rs117969779

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:44963615 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCTACCCCCGTCTTGTGGGAAAGA[C/G]AATTTATGGGAACAGCAGCTGCTAA

Phenotype

MIM: 600642

Polymorphism

C/G, Transversion 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		Intron			NP_149043.2
XM_017012503.1		Intron			XP_016867992.1
XM_017012504.1		Intron			XP_016867993.1

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