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SNP ID: rs113980525
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.13:78601914 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTCCGAGTCGCAGATGGACGCCAGG[C/T]CCGCTGCGCCCACCACGGCCGCCGC
Phenotype: MIM: 601632
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: LOC107987188 PubMed Links

Gene Details

Gene: LOC107987188
Gene Name: uncharacterized LOC107987188

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_017020899.1	995	Intron			XP_016876388.1

Gene: POU4F1
Gene Name: POU class 4 homeobox 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006237.3	995	Missense Mutation	GAC,GGC	D254G	NP_006228.3

Gene: RNF219-AS1
Gene Name: RNF219 antisense RNA 1

There are no transcripts associated with this gene.

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