Product Details

SNP ID: rs146862882
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.13:78601491 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAACCACACCCGCACCACGTTCTTT[C/T]TGAGGTCCAGTTTCTCGGCGATGGC
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	1418	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	1418	Missense Mutation	AAA,AGA	K395R	NP_006228.3

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

There are no transcripts associated with this gene.

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