Product Details

SNP ID

rs2004576

Assay Type

Functionally tested

NCBI dbSNP Submissions

17

Location

Chr.1:11488414 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCATCTCCTGGATGGACACCTGCT[C/T]CCCACTATCCATGCCTGAGCTGTCA

Phenotype

MIM: 611251

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

DISP3 PubMed Links

Gene Details

Gene

DISP3

Gene Name

dispatched RND transporter family member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020780.1		Intron			NP_065831.1
XM_011541828.2		Intron			XP_011540130.1
XM_011541829.1		Intron			XP_011540131.1
XM_011541830.2		Intron			XP_011540132.1
XM_011541831.2		Intron			XP_011540133.1
XM_011541832.2		Intron			XP_011540134.1
XM_011541833.2		Intron			XP_011540135.1
XM_011541835.2		Intron			XP_011540137.1

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