Product Details

SNP ID
rs11793308
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:34400583 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCCGGGGCTTGGGAGTTCATGGCTT[C/T]GCTGGGGTGGGGCCAAGCCCCTGGC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C9orf24 PubMed Links

Gene Details

Gene
C9orf24
Gene Name
chromosome 9 open reading frame 24
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001252195.1 251 Intron NP_001239124.1
NM_032596.3 251 Intron NP_115985.2
NM_147168.1 251 Intron NP_671697.1
NM_147169.2 251 Intron NP_671698.1
XM_005251616.4 251 UTR 5 XP_005251673.1
XM_005251618.4 251 Intron XP_005251675.1
XM_011518055.2 251 Intron XP_011516357.1
Gene
FAM219A
Gene Name
family with sequence similarity 219 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001184940.1 251 UTR 3 NP_001171869.1
NM_001184941.1 251 UTR 3 NP_001171870.1
NM_001184942.1 251 UTR 3 NP_001171871.1
NM_001184943.1 251 UTR 3 NP_001171872.1
NM_001184945.1 251 UTR 3 NP_001171874.1
NM_147202.1 251 UTR 3 NP_671735.1
XM_005251402.4 251 UTR 3 XP_005251459.1
XM_011517797.2 251 UTR 3 XP_011516099.1
XM_011517798.2 251 UTR 3 XP_011516100.1
XM_011517799.2 251 UTR 3 XP_011516101.1

View Full Product Details