Product Details

SNP ID

rs10205398

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:62453018 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCAGAGGCCTGCTGCCTCCCTGATG[C/T]CTGTCCATAAAGCAGGGTGGGAGAG

Phenotype

MIM: 614950

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TMEM17 PubMed Links

Gene Details

Gene

TMEM17

Gene Name

transmembrane protein 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198276.2	1332	Intron			NP_938017.2
XM_011532693.2	1332	Intron			XP_011530995.1
XM_011532694.2	1332	UTR 3			XP_011530996.1
XM_017003575.1	1332	Intron			XP_016859064.1

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