Product Details

SNP ID

rs201910426

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:218386641 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATCATCTCCTCCCCATAGGTGCCC[C/T]GCACCGTCCTCTGGCTGACCATCGA

Phenotype

MIM: 600266

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC11A1 PubMed Links

Gene Details

Gene

SLC11A1

Gene Name

solute carrier family 11 member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000578.3	1077	Missense Mutation	CGC,TGC	R134C	NP_000569.3
XM_005246793.3	1077	Missense Mutation	CGC,TGC	R67C	XP_005246850.1
XM_005246794.3	1077	Missense Mutation	CGC,TGC	R16C	XP_005246851.1
XM_006712709.3	1077	Missense Mutation	CGC,TGC	R16C	XP_006712772.1
XM_006712710.3	1077	Missense Mutation	CGC,TGC	R16C	XP_006712773.1
XM_006712711.3	1077	UTR 5			XP_006712774.1
XM_011511684.2	1077	Missense Mutation	CCG,CTG	P13L	XP_011509986.1
XM_011511685.2	1077	Missense Mutation	CCG,CTG	P13L	XP_011509987.1
XM_017004765.1	1077	Missense Mutation	CGC,TGC	R93C	XP_016860254.1
XM_017004766.1	1077	Missense Mutation	CGC,TGC	R67C	XP_016860255.1
XM_017004767.1	1077	Missense Mutation	CGC,TGC	R134C	XP_016860256.1

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