Product Details

SNP ID
rs142351795
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:235177803 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAATTAGAGATTTCACACTTACTGC[A/C]TTTTCCCTTCTTTTTGTTGTTTACC
Phenotype
MIM: 609696
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
ARID4B PubMed Links

Gene Details

Gene
ARID4B
Gene Name
AT-rich interaction domain 4B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001206794.1 3604 Missense Mutation GGC,TGC G1149C NP_001193723.1
NM_016374.5 3604 Missense Mutation GGC,TGC G1149C NP_057458.4
NM_031371.3 3604 Missense Mutation GGC,TGC G1063C NP_112739.2
XM_006711781.2 3604 Missense Mutation GGC,TGC G1113C XP_006711844.1
XM_011544212.2 3604 Missense Mutation GGC,TGC G1149C XP_011542514.1
XM_017001468.1 3604 Missense Mutation GGC,TGC G1151C XP_016856957.1
XM_017001469.1 3604 Missense Mutation GGC,TGC G1115C XP_016856958.1
XM_017001470.1 3604 Missense Mutation GGC,TGC G1065C XP_016856959.1
XM_017001471.1 3604 UTR 3 XP_016856960.1
XM_017001472.1 3604 Missense Mutation GGC,TGC G856C XP_016856961.1

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