Product Details

SNP ID

rs141450282

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:63163897 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTTCCACATCCTGGATGCTGTCA[A/G]GAAGAGGCTGGTTCCTGGTTTCAGG

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	1700	Missense Mutation	CCT,CTT	P524L	NP_955384.3
XM_017017684.1	1700	Missense Mutation	CCT,CTT	P554L	XP_016873173.1
XM_017017685.1	1700	Missense Mutation	CCT,CTT	P554L	XP_016873174.1
XM_017017686.1	1700	Missense Mutation	CCT,CTT	P554L	XP_016873175.1
XM_017017687.1	1700	Missense Mutation	CCT,CTT	P524L	XP_016873176.1
XM_017017688.1	1700	Missense Mutation	CCT,CTT	P454L	XP_016873177.1
XM_017017689.1	1700	Missense Mutation	CCT,CTT	P443L	XP_016873178.1
XM_017017690.1	1700	Missense Mutation	CCT,CTT	P429L	XP_016873179.1
XM_017017691.1	1700	Missense Mutation	CCT,CTT	P429L	XP_016873180.1
XM_017017692.1	1700	Missense Mutation	CCT,CTT	P382L	XP_016873181.1
XM_017017693.1	1700	Missense Mutation	CCT,CTT	P358L	XP_016873182.1
XM_017017694.1	1700	Missense Mutation	CCT,CTT	P356L	XP_016873183.1
XM_017017695.1	1700	Intron			XP_016873184.1
XM_017017696.1	1700	Missense Mutation	CCT,CTT	P293L	XP_016873185.1

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