Product Details

SNP ID
rs55806270
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:4898730 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGATGGGTGGGAAATTGAAGTCGG[C/T]GCGAGCTAAGGCTGGATACACGGCG
Phenotype
MIM: 100725 MIM: 609426
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C17orf107 PubMed Links

Gene Details

Gene
C17orf107
Gene Name
chromosome 17 open reading frame 107
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145536.1 1518 Intron NP_001139008.1
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 1518 UTR 3 NP_000071.1
XM_017024115.1 1518 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 1518 Intron NP_001020108.1
NM_001321236.1 1518 Intron NP_001308165.1
NM_015716.4 1518 Intron NP_056531.1
NM_153827.4 1518 Intron NP_722549.2
NM_170663.4 1518 Intron NP_733763.1
XM_006721531.2 1518 Intron XP_006721594.1
XM_006721532.2 1518 Intron XP_006721595.1
XM_006721536.2 1518 Intron XP_006721599.1
XM_011523906.1 1518 Intron XP_011522208.1
XM_017024704.1 1518 Intron XP_016880193.1
XM_017024705.1 1518 Intron XP_016880194.1
XM_017024706.1 1518 Intron XP_016880195.1
XM_017024707.1 1518 Intron XP_016880196.1
XM_017024708.1 1518 Intron XP_016880197.1

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