Product Details

SNP ID
rs11880463
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:5995259 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGGGGTCCTCCCACCCGCATGGG[A/G]CAGAGACGGGGCCCGGGGGTCCCTC
Phenotype
MIM: 142765
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LOC100128568 PubMed Links

Gene Details

Gene
LOC100128568
Gene Name
uncharacterized LOC100128568
There are no transcripts associated with this gene.

Gene
RFX2
Gene Name
regulatory factor X2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000635.3 Intron NP_000626.2
NM_134433.2 Intron NP_602309.1
XM_011528171.2 Intron XP_011526473.1
XM_011528172.1 Intron XP_011526474.1
XM_017027107.1 Intron XP_016882596.1
XM_017027108.1 Intron XP_016882597.1

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