Product Details

SNP ID

rs200478682

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:7042350 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCACGGCCACCACCAGCGCTGCTC[C/T]GTATCCCCCCAGGCCCCGGTCTAAA

Phenotype

MIM: 615765

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC16A11 PubMed Links

Gene Details

Gene

SLC16A11

Gene Name

solute carrier family 16 member 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153357.1	1403	Missense Mutation	AGA,GGA	R278G	NP_699188.1
XM_005256488.3	1403	Missense Mutation	AGA,GGA	R373G	XP_005256545.2
XM_017024281.1	1403	Missense Mutation	AGA,GGA	R373G	XP_016879770.1
XM_017024282.1	1403	Intron			XP_016879771.1

Gene

SLC16A13

Gene Name

solute carrier family 16 member 13

There are no transcripts associated with this gene.

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