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SNP ID: rs12587546
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.14:65004113 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: CTAAGCCTGTCATCCTGCAGAACCC[A/G]TCTTACAGTACTGTGAAGTTCCAGA
Phenotype: MIM: 134636 MIM: 154950
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CHURC1-FNTB PubMed Links

Gene Details

Gene: CHURC1-FNTB
Gene Name: CHURC1-FNTB readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001202558.1		Intron			NP_001189487.1
NM_001202559.1		Intron			NP_001189488.1

Gene: FNTB
Gene Name: farnesyltransferase, CAAX box, beta

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002028.3		Intron			NP_002019.1

Gene: MAX
Gene Name: MYC associated factor X

There are no transcripts associated with this gene.

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