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See other INTS10 GT Assays ›
SNP ID:
rs7822495
Gene
INTS10
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.8: 19820404 - 19820404 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

GTTTATTTGAAACTCTTCCTGGTCG[A/G]GTCCAGTGTGAAATGTTACTAAAGG

Assay ID C__25956664_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: 611353

Literature Links:

 INTS10 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.24)
(0.76)
Caucasian - Not Available CEPH (CEU)
A (0.14)
(0.86)
EAS
A (0.29)
(0.71)
African American - Not Available YRI (Yoruba)
A (0.32)
(0.68)
SAS
A (0.20)
(0.80)
Chinese - Not Available JPT (Japanese)
A (0.19)
(0.81)
AFR
A (0.28)
(0.72)
Japanese - Not Available CHB (Han Chinese)
A (0.31)
(0.69)
EUR
A (0.17)
(0.83)
AMR
A (0.28)
(0.72)
INTS10 - integrator complex subunit 10
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_018142.2 281 Silent Mutation CGA,CGG R,R 109 NP_060612.2
XM_005273555.3 281 Silent Mutation CGA,CGG R,R 109 XP_005273612.1
XM_005273556.3 281 Silent Mutation CGA,CGG R,R 109 XP_005273613.1
XM_005273557.3 281 Silent Mutation CGA,CGG R,R 109 XP_005273614.1
XM_006716355.2 281 UTR 5 XP_006716418.1
XM_017013606.1 281 Silent Mutation CGA,CGG R,R 109 XP_016869095.1
XM_017013607.1 281 Silent Mutation CGA,CGG R,R 109 XP_016869096.1
XM_017013608.1 281 UTR 5 XP_016869097.1
XM_017013609.1 281 UTR 5 XP_016869098.1

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