Product Details

SNP ID

rs201100362

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:140363045 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACAGCCCGGATTCCCCCGCCCAAAT[A/G]TCTGCCATCTCAGCACAAAAGGTAC

Phenotype

MIM: 610207

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC4A9 PubMed Links

Gene Details

Gene

SLC4A9

Gene Name

solute carrier family 4 member 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001258426.1	976	Missense Mutation	TAT,TGT	Y314C	NP_001245355.1
NM_001258427.1	976	Missense Mutation	TAT,TGT	Y314C	NP_001245356.1
NM_001258428.1	976	Missense Mutation	TAT,TGT	Y338C	NP_001245357.1
NM_031467.2	976	Missense Mutation	TAT,TGT	Y314C	NP_113655.2
XM_005268521.3	976	Missense Mutation	TAT,TGT	Y338C	XP_005268578.2
XM_011537694.2	976	Missense Mutation	TAT,TGT	Y362C	XP_011535996.1
XM_017009933.1	976	Missense Mutation	TAT,TGT	Y362C	XP_016865422.1
XM_017009934.1	976	Missense Mutation	TAT,TGT	Y362C	XP_016865423.1
XM_017009935.1	976	Missense Mutation	TAT,TGT	Y362C	XP_016865424.1
XM_017009936.1	976	Missense Mutation	TAT,TGT	Y338C	XP_016865425.1
XM_017009937.1	976	Missense Mutation	TAT,TGT	Y324C	XP_016865426.1
XM_017009938.1	976	Missense Mutation	TAT,TGT	Y362C	XP_016865427.1
XM_017009939.1	976	Missense Mutation	TAT,TGT	Y338C	XP_016865428.1
XM_017009940.1	976	Missense Mutation	TAT,TGT	Y362C	XP_016865429.1
XM_017009941.1	976	Missense Mutation	TAT,TGT	Y362C	XP_016865430.1
XM_017009942.1	976	Missense Mutation	TAT,TGT	Y362C	XP_016865431.1
XM_017009943.1	976	Missense Mutation	TAT,TGT	Y300C	XP_016865432.1

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