Product Details

SNP ID: rs111413086
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:1313368 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAAGCGCCTCAGCCACCGCGCGCCG[A/G]TCCCCGCGCCCGGGCTGCGGCCCGA
Phenotype: MIM: 612788
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: FOXQ1 PubMed Links

Gene Details

Gene: FOXQ1
Gene Name: forkhead box Q1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033260.3	929	Missense Mutation	ATC,GTC	I222V	NP_150285.3

Gene: LINC01394
Gene Name: long intergenic non-protein coding RNA 1394

There are no transcripts associated with this gene.

Gene: LOC107986554
Gene Name: uncharacterized LOC107986554

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_017011607.1	929	Intron			XP_016867096.1
XM_017011608.1	929	Intron			XP_016867097.1
XM_017011609.1	929	Intron			XP_016867098.1
XM_017011610.1	929	Intron			XP_016867099.1
XM_017011611.1	929	Intron			XP_016867100.1

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