Product Details

SNP ID

rs77913769

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:89432902 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGGCTAGTCCAGCTTTCCTTATT[A/T]TGTGCTGTTTTCCCTTATAAATATT

Phenotype

MIM: 611910

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

SLC16A12 PubMed Links

Gene Details

Gene

SLC16A12

Gene Name

solute carrier family 16 member 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_213606.3	1902	UTR 3			NP_998771.3
XM_017016237.1	1902	UTR 3			XP_016871726.1
XM_017016238.1	1902	UTR 3			XP_016871727.1
XM_017016239.1	1902	UTR 3			XP_016871728.1

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