Product Details
- SNP ID
-
rs183404476
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:63164544 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTTGTACCTGATTATGGAAGGAATT[A/G]GTTCATTTTCTTGGGCAGTAGAACA
- Phenotype
-
MIM: 610792
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SLC22A25
PubMed Links
Gene Details
- Gene
- SLC22A25
- Gene Name
- solute carrier family 22 member 25
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_199352.3 |
1505 |
Missense Mutation |
CCA,CTA |
P459L |
NP_955384.3 |
| XM_017017684.1 |
1505 |
Missense Mutation |
CCA,CTA |
P489L |
XP_016873173.1 |
| XM_017017685.1 |
1505 |
Missense Mutation |
CCA,CTA |
P489L |
XP_016873174.1 |
| XM_017017686.1 |
1505 |
Missense Mutation |
CCA,CTA |
P489L |
XP_016873175.1 |
| XM_017017687.1 |
1505 |
Missense Mutation |
CCA,CTA |
P459L |
XP_016873176.1 |
| XM_017017688.1 |
1505 |
Missense Mutation |
CCA,CTA |
P389L |
XP_016873177.1 |
| XM_017017689.1 |
1505 |
Missense Mutation |
CCA,CTA |
P378L |
XP_016873178.1 |
| XM_017017690.1 |
1505 |
Missense Mutation |
CCA,CTA |
P364L |
XP_016873179.1 |
| XM_017017691.1 |
1505 |
Missense Mutation |
CCA,CTA |
P364L |
XP_016873180.1 |
| XM_017017692.1 |
1505 |
Missense Mutation |
CCA,CTA |
P317L |
XP_016873181.1 |
| XM_017017693.1 |
1505 |
Missense Mutation |
CCA,CTA |
P293L |
XP_016873182.1 |
| XM_017017694.1 |
1505 |
Missense Mutation |
CCA,CTA |
P291L |
XP_016873183.1 |
| XM_017017695.1 |
1505 |
Intron |
|
|
XP_016873184.1 |
| XM_017017696.1 |
1505 |
Missense Mutation |
CCA,CTA |
P228L |
XP_016873185.1 |
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