Product Details
- SNP ID
-
rs201910426
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:218386641 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GATCATCTCCTCCCCATAGGTGCCC[C/T]GCACCGTCCTCTGGCTGACCATCGA
- Phenotype
-
MIM: 600266
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SLC11A1
PubMed Links
Gene Details
- Gene
- SLC11A1
- Gene Name
- solute carrier family 11 member 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_000578.3 |
1077 |
Missense Mutation |
CGC,TGC |
R134C |
NP_000569.3 |
XM_005246793.3 |
1077 |
Missense Mutation |
CGC,TGC |
R67C |
XP_005246850.1 |
XM_005246794.3 |
1077 |
Missense Mutation |
CGC,TGC |
R16C |
XP_005246851.1 |
XM_006712709.3 |
1077 |
Missense Mutation |
CGC,TGC |
R16C |
XP_006712772.1 |
XM_006712710.3 |
1077 |
Missense Mutation |
CGC,TGC |
R16C |
XP_006712773.1 |
XM_006712711.3 |
1077 |
UTR 5 |
|
|
XP_006712774.1 |
XM_011511684.2 |
1077 |
Missense Mutation |
CCG,CTG |
P13L |
XP_011509986.1 |
XM_011511685.2 |
1077 |
Missense Mutation |
CCG,CTG |
P13L |
XP_011509987.1 |
XM_017004765.1 |
1077 |
Missense Mutation |
CGC,TGC |
R93C |
XP_016860254.1 |
XM_017004766.1 |
1077 |
Missense Mutation |
CGC,TGC |
R67C |
XP_016860255.1 |
XM_017004767.1 |
1077 |
Missense Mutation |
CGC,TGC |
R134C |
XP_016860256.1 |
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