Product Details
- SNP ID
-
rs74587373
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:65624338 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCCCTTCAAAACCTAGCTCCGAAAT[G/T]GGGGGTAAGATGCTGGTACCCCAAG
- Phenotype
-
MIM: 603617
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
SLC24A1
PubMed Links
Gene Details
- Gene
- SLC24A1
- Gene Name
- solute carrier family 24 member 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001254740.1 |
519 |
Intron |
|
|
NP_001241669.1 |
NM_001301031.1 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
NP_001287960.1 |
NM_001301032.1 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
NP_001287961.1 |
NM_001301033.1 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
NP_001287962.1 |
NM_004727.2 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
NP_004718.1 |
XM_005254778.3 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
XP_005254835.1 |
XM_005254781.3 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
XP_005254838.1 |
XM_006720768.3 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
XP_006720831.1 |
XM_011522219.1 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
XP_011520521.1 |
XM_011522220.2 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
XP_011520522.1 |
XM_011522221.2 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
XP_011520523.1 |
XM_011522222.2 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
XP_011520524.1 |
XM_011522226.2 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
XP_011520528.1 |
XM_017022724.1 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
XP_016878213.1 |
XM_017022725.1 |
519 |
Missense Mutation |
ATG,ATT |
M86I |
XP_016878214.1 |
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