Product Details

SNP ID
rs139682593
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:17800827 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGATGTGACTATCCATCATGGCT[A/G]GGGCCTCATGGGACGTGGCAGGGGC
Phenotype
MIM: 300217
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RAI2 PubMed Links

Gene Details

Gene
RAI2
Gene Name
retinoic acid induced 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001172732.1 1829 Missense Mutation CCA,CTA P345L NP_001166203.1
NM_001172739.1 1829 Missense Mutation CCA,CTA P395L NP_001166210.1
NM_001172743.1 1829 Missense Mutation CCA,CTA P395L NP_001166214.1
NM_021785.4 1829 Missense Mutation CCA,CTA P395L NP_068557.3
XM_006724459.2 1829 Missense Mutation CCA,CTA P395L XP_006724522.1
XM_006724460.1 1829 Missense Mutation CCA,CTA P395L XP_006724523.1
XM_011545439.2 1829 Missense Mutation CCA,CTA P395L XP_011543741.1
XM_011545440.2 1829 Missense Mutation CCA,CTA P395L XP_011543742.1
XM_011545441.2 1829 Missense Mutation CCA,CTA P395L XP_011543743.1

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