Product Details

SNP ID
rs200039195
Assay Type
Functionally tested
NCBI dbSNP Submissions
5
Location
Chr.1:235175210 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATCTGAAAACTCCATTTGTAAACT[C/T]TGGGTAATCGATTACTGGGTTCCTT
Phenotype
MIM: 609696
Polymorphism
C/T, 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 3797 Missense Mutation AAA,AGA K1213R NP_001193723.1
NM_016374.5 3797 Missense Mutation AAA,AGA K1213R NP_057458.4
NM_031371.3 3797 Missense Mutation AAA,AGA K1127R NP_112739.2
XM_006711781.2 3797 Missense Mutation AAA,AGA K1177R XP_006711844.1
XM_011544212.2 3797 Missense Mutation AAA,AGA K1213R XP_011542514.1
XM_017001468.1 3797 Missense Mutation AAA,AGA K1215R XP_016856957.1
XM_017001469.1 3797 Missense Mutation AAA,AGA K1179R XP_016856958.1
XM_017001470.1 3797 Missense Mutation AAA,AGA K1129R XP_016856959.1
XM_017001471.1 3797 Intron XP_016856960.1
XM_017001472.1 3797 Missense Mutation AAA,AGA K920R XP_016856961.1

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