Product Details

SNP ID
rs16995823
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:35546589 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGCATAAATGAAAGGATGAATGAAC[A/G]GATATTGAGTGAGTGAGTGGATGAA
Phenotype
MIM: 612842
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RASD2 PubMed Links

Gene Details

Gene
RASD2
Gene Name
RASD family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014310.3 2594 Intron NP_055125.2
XM_005261442.4 2594 Intron XP_005261499.1
XM_011530040.2 2594 Intron XP_011528342.1
XM_017028701.1 2594 UTR 5 XP_016884190.1
XM_017028702.1 2594 Intron XP_016884191.1

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