Product Details

SNP ID: rs2879097
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.17:38733306 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: CTGTGACGGCTCCCACTTCTTCCAA[C/T]GCACTGGCCTATCTCCACTCAAGTT
Phenotype: MIM: 611933 MIM: 600328 MIM: 600346
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CISD3 PubMed Links

Gene Details

Gene: CISD3
Gene Name: CDGSH iron sulfur domain 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136498.1	337	Missense Mutation	CGC,TGC	R79C	NP_001129970.1

Gene: MLLT6
Gene Name: MLLT6, PHD finger domain containing

There are no transcripts associated with this gene.

Gene: PCGF2
Gene Name: polycomb group ring finger 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007144.2	337	Intron			NP_009075.1
XM_005257640.2	337	Intron			XP_005257697.1
XM_005257641.4	337	Intron			XP_005257698.1
XM_005257642.3	337	Intron			XP_005257699.1
XM_017025016.1	337	Intron			XP_016880505.1

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