Product Details

SNP ID

rs140355561

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:27256802 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCGACTCACCTTCCATGAGGATT[C/G]GAAGAACGTCTCGGAGGGTGGGAGC

Phenotype

MIM: 602878

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC30A3 PubMed Links

Gene Details

Gene

SLC30A3

Gene Name

solute carrier family 30 member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318949.1	912	Missense Mutation	CCA,CGA	P285R	NP_001305878.1
NM_001318950.1	912	Missense Mutation	CCA,CGA	P277R	NP_001305879.1
NM_001318951.1	912	Missense Mutation	CCA,CGA	P277R	NP_001305880.1
NM_003459.4	912	Missense Mutation	CCA,CGA	P290R	NP_003450.2
XM_005264547.1	912	Missense Mutation	CAA,GAA	Q239E	XP_005264604.1
XM_005264548.3	912	Missense Mutation	CAA,GAA	Q234E	XP_005264605.1
XM_006712100.2	912	Missense Mutation	CAA,GAA	Q190E	XP_006712163.1
XM_011533102.2	912	Missense Mutation	CCA,CGA	P217R	XP_011531404.1
XM_011533103.2	912	Missense Mutation	CCA,CGA	P176R	XP_011531405.1
XM_017004873.1	912	Missense Mutation	CAA,GAA	Q226E	XP_016860362.1
XM_017004874.1	912	Missense Mutation	CAA,GAA	Q226E	XP_016860363.1
XM_017004875.1	912	Missense Mutation	CAA,GAA	Q217E	XP_016860364.1

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