Search

  • Contáctenos
  • Orden Rápida

System Message

OKCancel
LOADING ...
See other CISD3 GT Assays ›
SNP ID:
rs112908318
Gene
CISD3 MLLT6 PCGF2
Gene Name
Set Membership:
-
Chromosome Location:
Chr.17: 38735241 - 38735241 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

CCTGGCCTCAAGTTAAGGGGGGCAC[A/G]GGAGCGCCGTTGACAGTCATCTTGC

Assay ID C_153064239_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
Check your price ›

Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 611933 MIM: 600328 MIM: 600346

Literature Links:

 CISD3 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.00)
(1.00)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS
A (0.00)
(1.00)
African American - Not Available YRI (Yoruba) - Not Available
SAS
A (0.00)
(1.00)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
A (0.00)
(1.00)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
A (0.00)
(1.00)
AMR
A (0.00)
(1.00)
CISD3 - CDGSH iron sulfur domain 3
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001136498.1 2279 UTR 3 NP_001129970.1
MLLT6 - MLLT6, PHD finger domain containing
There are no transcripts associated with this gene.
PCGF2 - polycomb group ring finger 2
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_007144.2 2279 Silent Mutation CCC,CCT P,P 339 NP_009075.1
XM_005257640.2 2279 Silent Mutation CCC,CCT P,P 339 XP_005257697.1
XM_005257641.4 2279 Silent Mutation CCC,CCT P,P 339 XP_005257698.1
XM_005257642.3 2279 Silent Mutation CCC,CCT P,P 339 XP_005257699.1
XM_017025016.1 2279 Silent Mutation CCC,CCT P,P 339 XP_016880505.1

Back To Top

Related Products