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See other ADAMTS17 GT Assays ›
SNP ID:
rs981041
Gene
ADAMTS17
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.15: 100064941 - 100064941 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

TCTCAACTTAGATTACAAATCCTAG[C/T]CCTGTTGTTCCCAATGTGATCACCA

Assay ID C___8858726_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: 607511

Literature Links:

 ADAMTS17 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
C (0.12)
(0.88)
Caucasian - Not Available CEPH (CEU)
C (0.04)
(0.96)
EAS
C (0.06)
(0.94)
African American - Not Available YRI (Yoruba)
C (0.31)
(0.69)
SAS
C (0.03)
(0.97)
Chinese - Not Available JPT (Japanese)
C (0.08)
(0.92)
AFR
C (0.29)
(0.71)
Japanese - Not Available CHB (Han Chinese)
C (0.06)
(0.94)
EUR
C (0.07)
(0.93)
AMR
C (0.09)
(0.91)
ADAMTS17 - ADAM metallopeptidase with thrombospondin type 1 motif 17
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_139057.3 Intron NP_620688.2
XM_005254872.3 Intron XP_005254929.1
XM_011521312.2 Intron XP_011519614.1
XM_017021973.1 Intron XP_016877462.1
XM_017021974.1 Intron XP_016877463.1
XM_017021975.1 Intron XP_016877464.1
XM_017021976.1 Intron XP_016877465.1
XM_017021977.1 Intron XP_016877466.1
XM_017021978.1 Intron XP_016877467.1
XM_017021979.1 Intron XP_016877468.1
XM_017021980.1 Intron XP_016877469.1
XM_017021981.1 Intron XP_016877470.1
XM_017021982.1 Intron XP_016877471.1
XM_017021983.1 Intron XP_016877472.1
XM_017021984.1 Intron XP_016877473.1

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More Information


Set Membership:

 HapMap

Panther Classification:

Molecular Function -

metalloprotease

Gene Ontology Categories:

Function(s) Process(es)


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