Product Details

SNP ID
rs141415407
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:5994902 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTTACCAGGGGCTCACCCAGGCTG[A/C]GGGCGTCTGGGCCCGCCTCGCTGCC
Phenotype
MIM: 142765
Polymorphism
A/C, Transversion 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 2149 Missense Mutation NP_000626.2
NM_134433.2 2149 Missense Mutation NP_602309.1
XM_011528171.2 2149 Missense Mutation XP_011526473.1
XM_011528172.1 2149 UTR 3 XP_011526474.1
XM_017027107.1 2149 Missense Mutation XP_016882596.1
XM_017027108.1 2149 Missense Mutation XP_016882597.1

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