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SNP ID: rs151006465
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:4900849 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTGGGATTTTCTGGGCAATGAGGAA[A/C]AAGAAGACGGTCTGGGCGAGCAGGA
Phenotype: MIM: 100725 MIM: 609426
Polymorphism: A/C, Transversion 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	891	UTR 3			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	891	Missense Mutation	TTG,TTT	L287F	NP_000071.1
XM_017024115.1	891	Missense Mutation	TTG,TTT	L275F	XP_016879604.1

Gene: MINK1
Gene Name: misshapen like kinase 1

There are no transcripts associated with this gene.

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