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See other TNFRSF10B GT Assays ›
SNP ID:
rs4428669
Gene
TNFRSF10B
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.8: 23038267 - 23038267 on Build GRCh38
Polymorphism:
T/A, Transversion substitution
Context Sequence [VIC/FAM]:

ACGACCCTATTAAAGCAGGACCACT[T/A]ATAGCTCAGACCCTTCAGGAATAAA

Assay ID C__28029126_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 603612

Literature Links:

 TNFRSF10B PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.14)
(0.86)
Caucasian - Not Available CEPH (CEU)
A (0.10)
(0.90)
EAS
A (0.01)
(0.99)
African American - Not Available YRI (Yoruba)
A (0.34)
(0.66)
SAS
A (0.14)
(0.86)
Chinese - Not Available JPT (Japanese)
A (0.02)
(0.98)
AFR
A (0.29)
(0.71)
Japanese - Not Available CHB (Han Chinese)
A (0.02)
(0.98)
EUR
A (0.10)
(0.90)
AMR
A (0.12)
(0.88)
TNFRSF10B - TNF receptor superfamily member 10b
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_003842.4 Intron NP_003833.4
NM_147187.2 Intron NP_671716.2
XM_017013944.1 Intron XP_016869433.1

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