Product Details

SNP ID
hCV25999706
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:44965107 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCGCCACCTGGGAGAGGGCATGTA[C/G]TCAGACAGATGCTGGCCATGTGTTC
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

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