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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