Product Details

SNP ID
rs199556870
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:235177907 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCATCTTTCACTCTTTTCTGACCT[A/G]TACAGGCTATGAAGGGAAAGGAATT
Phenotype
MIM: 609696
Polymorphism
A/G, Transition 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 3500 Missense Mutation ACA,ATA T1114I NP_001193723.1
NM_016374.5 3500 Missense Mutation ACA,ATA T1114I NP_057458.4
NM_031371.3 3500 Missense Mutation ACA,ATA T1028I NP_112739.2
XM_006711781.2 3500 Missense Mutation ACA,ATA T1078I XP_006711844.1
XM_011544212.2 3500 Missense Mutation ACA,ATA T1114I XP_011542514.1
XM_017001468.1 3500 Missense Mutation ACA,ATA T1116I XP_016856957.1
XM_017001469.1 3500 Missense Mutation ACA,ATA T1080I XP_016856958.1
XM_017001470.1 3500 Missense Mutation ACA,ATA T1030I XP_016856959.1
XM_017001471.1 3500 UTR 3 XP_016856960.1
XM_017001472.1 3500 Missense Mutation ACA,ATA T821I XP_016856961.1

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