Product Details

SNP ID

rs142672835

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:43306257 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGCAGTCAGGGTCTTGTGGCAAC[A/G]CTGGCACCTCAGACACGGTCGGTGC

Phenotype

MIM: 604995

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CRIP3 PubMed Links

Gene Details

Gene

CRIP3

Gene Name

cysteine rich protein 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_206922.2	457	Missense Mutation			NP_996805.2
XM_005249103.3	457	Missense Mutation			XP_005249160.1
XM_011514609.2	457	Missense Mutation			XP_011512911.1
XM_017010856.1	457	Missense Mutation			XP_016866345.1
XM_017010857.1	457	Missense Mutation			XP_016866346.1

Gene

SLC22A7

Gene Name

solute carrier family 22 member 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006672.3	457	Intron			NP_006663.2
NM_153320.2	457	Intron			NP_696961.2
XM_006714970.3	457	Intron			XP_006715033.1
XM_006714971.3	457	Intron			XP_006715034.1
XM_011514256.2	457	Intron			XP_011512558.1
XM_011514257.2	457	Intron			XP_011512559.1
XM_011514259.1	457	Intron			XP_011512561.1
XM_011514261.2	457	Intron			XP_011512563.1
XM_011514262.2	457	Intron			XP_011512564.1
XM_011514263.2	457	Intron			XP_011512565.1
XM_017010198.1	457	Intron			XP_016865687.1
XM_017010199.1	457	Intron			XP_016865688.1
XM_017010200.1	457	Intron			XP_016865689.1
XM_017010201.1	457	Intron			XP_016865690.1

View Full Product Details