Product Details

SNP ID

rs200844376

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:63163930 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGTTCCTGGTTTCAGGAAGGAGG[A/G]GGACAACAAGGCCAGAGAGGATGGC

Phenotype

MIM: 610792

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC22A25 PubMed Links

Gene Details

Gene

SLC22A25

Gene Name

solute carrier family 22 member 25

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_199352.3	1667	Missense Mutation	CCC,CTC	P513L	NP_955384.3
XM_017017684.1	1667	Missense Mutation	CCC,CTC	P543L	XP_016873173.1
XM_017017685.1	1667	Missense Mutation	CCC,CTC	P543L	XP_016873174.1
XM_017017686.1	1667	Missense Mutation	CCC,CTC	P543L	XP_016873175.1
XM_017017687.1	1667	Missense Mutation	CCC,CTC	P513L	XP_016873176.1
XM_017017688.1	1667	Missense Mutation	CCC,CTC	P443L	XP_016873177.1
XM_017017689.1	1667	Missense Mutation	CCC,CTC	P432L	XP_016873178.1
XM_017017690.1	1667	Missense Mutation	CCC,CTC	P418L	XP_016873179.1
XM_017017691.1	1667	Missense Mutation	CCC,CTC	P418L	XP_016873180.1
XM_017017692.1	1667	Missense Mutation	CCC,CTC	P371L	XP_016873181.1
XM_017017693.1	1667	Missense Mutation	CCC,CTC	P347L	XP_016873182.1
XM_017017694.1	1667	Missense Mutation	CCC,CTC	P345L	XP_016873183.1
XM_017017695.1	1667	Intron			XP_016873184.1
XM_017017696.1	1667	Missense Mutation	CCC,CTC	P282L	XP_016873185.1

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