Product Details

SNP ID: rs12936083
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:4898592 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CGGCCAGGCCTACACACGCCAGGGA[A/G]CGGGCACACACCATTCTTGTGAAGT
Phenotype: MIM: 100725 MIM: 609426
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: C17orf107 PubMed Links

Gene Details

Gene: C17orf107
Gene Name: chromosome 17 open reading frame 107

There are no transcripts associated with this gene.

Gene: CHRNE
Gene Name: cholinergic receptor nicotinic epsilon subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000080.3	1656	UTR 3			NP_000071.1
XM_017024115.1	1656	UTR 3			XP_016879604.1

Gene: MINK1
Gene Name: misshapen like kinase 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001024937.3	1656	Intron			NP_001020108.1
NM_001321236.1	1656	Intron			NP_001308165.1
NM_015716.4	1656	Intron			NP_056531.1
NM_153827.4	1656	Intron			NP_722549.2
NM_170663.4	1656	Intron			NP_733763.1
XM_006721531.2	1656	Intron			XP_006721594.1
XM_006721532.2	1656	Intron			XP_006721595.1
XM_006721536.2	1656	Intron			XP_006721599.1
XM_011523906.1	1656	Intron			XP_011522208.1
XM_017024704.1	1656	Intron			XP_016880193.1
XM_017024705.1	1656	Intron			XP_016880194.1
XM_017024706.1	1656	Intron			XP_016880195.1
XM_017024707.1	1656	Intron			XP_016880196.1
XM_017024708.1	1656	Intron			XP_016880197.1

View Full Product Details