Product Details
- SNP ID
-
rs73625098
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:43298659 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CACGTTGGGGGAAGAAAGGCAGAGC[C/T]GTGGGGAGCTGGAGGATGAACCTGC
- Phenotype
-
MIM: 604995
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CRIP3
PubMed Links
Gene Details
- Gene
- CRIP3
- Gene Name
- cysteine rich protein 3
There are no transcripts associated with this gene.
- 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 |
400 |
Missense Mutation |
CGT,TGT |
R101C |
NP_006663.2 |
NM_153320.2 |
400 |
Missense Mutation |
CGT,TGT |
R101C |
NP_696961.2 |
XM_006714970.3 |
400 |
Missense Mutation |
CGT,TGT |
R101C |
XP_006715033.1 |
XM_006714971.3 |
400 |
Missense Mutation |
CGT,TGT |
R101C |
XP_006715034.1 |
XM_011514256.2 |
400 |
Missense Mutation |
CGT,TGT |
R101C |
XP_011512558.1 |
XM_011514257.2 |
400 |
Missense Mutation |
CGT,TGT |
R101C |
XP_011512559.1 |
XM_011514259.1 |
400 |
Missense Mutation |
CGT,TGT |
R101C |
XP_011512561.1 |
XM_011514261.2 |
400 |
UTR 5 |
|
|
XP_011512563.1 |
XM_011514262.2 |
400 |
Missense Mutation |
CGT,TGT |
R101C |
XP_011512564.1 |
XM_011514263.2 |
400 |
UTR 5 |
|
|
XP_011512565.1 |
XM_017010198.1 |
400 |
Missense Mutation |
CGT,TGT |
R101C |
XP_016865687.1 |
XM_017010199.1 |
400 |
Missense Mutation |
CGT,TGT |
R101C |
XP_016865688.1 |
XM_017010200.1 |
400 |
Missense Mutation |
CGT,TGT |
R34C |
XP_016865689.1 |
XM_017010201.1 |
400 |
UTR 5 |
|
|
XP_016865690.1 |
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