Product Details

SNP ID
rs79607088
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:65660552 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATAACTAATTCTAGCAGCCAAAAGA[A/T]GTTTTTCCTTACCAGAAATTACCCA
Phenotype
MIM: 600382 MIM: 603617
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
DENND4A PubMed Links

Gene Details

Gene
DENND4A
Gene Name
DENN domain containing 4A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001144823.2 7269 UTR 3 NP_001138295.1
NM_001320835.1 7269 UTR 3 NP_001307764.1
NM_005848.4 7269 UTR 3 NP_005839.3
XM_005254120.4 7269 UTR 3 XP_005254177.1
XM_005254121.3 7269 UTR 3 XP_005254178.1
XM_005254122.4 7269 UTR 3 XP_005254179.1
XM_006720371.3 7269 UTR 3 XP_006720434.1
XM_011521156.2 7269 Intron XP_011519458.1
XM_011521157.2 7269 UTR 3 XP_011519459.1
XM_017021862.1 7269 UTR 3 XP_016877351.1
XM_017021863.1 7269 UTR 3 XP_016877352.1
XM_017021864.1 7269 Intron XP_016877353.1
XM_017021865.1 7269 UTR 3 XP_016877354.1
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 7269 Intron NP_001241669.1
NM_001301031.1 7269 Intron NP_001287960.1
NM_001301032.1 7269 Intron NP_001287961.1
NM_001301033.1 7269 Intron NP_001287962.1
NM_004727.2 7269 Intron NP_004718.1
XM_005254778.3 7269 Intron XP_005254835.1
XM_005254781.3 7269 Intron XP_005254838.1
XM_006720768.3 7269 Intron XP_006720831.1
XM_011522219.1 7269 Intron XP_011520521.1
XM_011522220.2 7269 Intron XP_011520522.1
XM_011522221.2 7269 Intron XP_011520523.1
XM_011522222.2 7269 Intron XP_011520524.1
XM_011522226.2 7269 Intron XP_011520528.1
XM_017022724.1 7269 Intron XP_016878213.1
XM_017022725.1 7269 Intron XP_016878214.1

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