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SNP ID: rs12269028
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:45000672 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GTACCAGGGTCTCAAAAATCTCAAA[A/T]TTTGTGGAAAGTATGCAGTTTCTAG
Phenotype: MIM: 610559 MIM: 194529
Polymorphism: A/T, Transversion substitution
Allele Nomenclature
Literature Links: C10orf25 PubMed Links

Gene Details

Gene: C10orf25
Gene Name: chromosome 10 open reading frame 25

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039380.3	239	Missense Mutation	AAT,ATT	N63I	NP_001034469.2
XM_017015895.1	239	Missense Mutation	AAT,ATT	N63I	XP_016871384.1

Gene: RASSF4
Gene Name: Ras association domain family member 4

There are no transcripts associated with this gene.

Gene: ZNF22
Gene Name: zinc finger protein 22

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006963.4	239	Intron			NP_008894.2

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