Product Details

SNP ID
rs1001192
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:146257824 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCAGGCTGGCCCAAGATCCATCCT[C/T]TGAACCAGGTAGAGGATAGGATGTG
Phenotype
MIM: 611459
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC10A7 PubMed Links

Gene Details

Gene
SLC10A7
Gene Name
solute carrier family 10 member 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001029998.5 Intron NP_001025169.1
NM_001300842.2 Intron NP_001287771.1
NM_001317816.1 Intron NP_001304745.1
NM_001317817.1 Intron NP_001304746.1
NM_001317818.1 Intron NP_001304747.1
NM_032128.4 Intron NP_115504.1
XM_011532311.2 Intron XP_011530613.1
XM_011532313.2 Intron XP_011530615.1
XM_011532314.2 Intron XP_011530616.1
XM_017008689.1 Intron XP_016864178.1
XM_017008690.1 Intron XP_016864179.1
XM_017008691.1 Intron XP_016864180.1
XM_017008692.1 Intron XP_016864181.1

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