Product Details

SNP ID

rs722651

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:13106336 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATAAAATTTAGGGACATTGCTTCAT[A/G]TATTTGCCATTTACTCAATTGTAGA

Phenotype

MIM: 603785

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MPDZ PubMed Links

Gene Details

Gene

MPDZ

Gene Name

multiple PDZ domain crumbs cell polarity complex component

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001261406.1	6977	UTR 3			NP_001248335.1
NM_001261407.1	6977	UTR 3			NP_001248336.1
NM_003829.4	6977	UTR 3			NP_003820.2
XM_005251622.4	6977	UTR 3			XP_005251679.1
XM_005251623.4	6977	UTR 3			XP_005251680.1
XM_006716885.3	6977	UTR 3			XP_006716948.1
XM_006716886.3	6977	UTR 3			XP_006716949.1
XM_006716887.3	6977	UTR 3			XP_006716950.1
XM_006716888.3	6977	UTR 3			XP_006716951.1
XM_006716889.3	6977	UTR 3			XP_006716952.1
XM_006716891.3	6977	UTR 3			XP_006716954.1
XM_017015252.1	6977	UTR 3			XP_016870741.1
XM_017015253.1	6977	UTR 3			XP_016870742.1
XM_017015254.1	6977	UTR 3			XP_016870743.1
XM_017015255.1	6977	UTR 3			XP_016870744.1
XM_017015256.1	6977	UTR 3			XP_016870745.1
XM_017015257.1	6977	UTR 3			XP_016870746.1
XM_017015258.1	6977	Intron			XP_016870747.1
XM_017015259.1	6977	Intron			XP_016870748.1

View Full Product Details