Product Details

SNP ID: rs9611564
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:41369140 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCCAGTGGGGCAGGGAGGATTCTCA[C/G]GGGCGACTCGGGGCACTGCTCCTCA
Phenotype: MIM: 188595
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: LOC100996598 PubMed Links

Gene Details

Gene: LOC100996598
Gene Name: uncharacterized LOC100996598

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_017029163.1	59	Missense Mutation	ACG,AGG	T20R	XP_016884652.1

Gene: TEF
Gene Name: TEF, PAR bZIP transcription factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145398.2	59	Intron			NP_001138870.1
NM_003216.3	59	Intron			NP_003207.1

Gene: ZC3H7B
Gene Name: zinc finger CCCH-type containing 7B

There are no transcripts associated with this gene.

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