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SNP ID:
rs1565073
Gene
DOCK10
Gene Name
Set Membership:
> HapMap > Validated
Chromosome Location:
Chr.2: 224769976 - 224769976 on Build GRCh38
Polymorphism:
G/T, Transversion substitution
Context Sequence [VIC/FAM]:

ATAGTCTAGAAAACCCAGGGTTCAT[G/T]TGGACTGTGGAAAGTATCTAGGTTC

Assay ID C___8720778_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 611518

Literature Links:

 DOCK10 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.31)
(0.69)
Caucasian
G (0.43)
(0.57)
CEPH (CEU)
T (0.49)
(0.51)
EAS
T (0.27)
(0.73)
African American
T (0.23)
(0.77)
YRI (Yoruba)
T (0.14)
(0.86)
SAS
T (0.34)
(0.66)
Japanese
T (0.32)
(0.68)
JPT (Japanese)
T (0.30)
(0.70)
AFR
T (0.14)
(0.86)
Chinese
T (0.26)
(0.74)
CHB (Han Chinese)
T (0.22)
(0.78)
EUR
G (0.50)
(0.50)
AMR
T (0.41)
(0.59)
DOCK10 - dedicator of cytokinesis 10
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001290263.1 6994 Intron NP_001277192.1
NM_014689.2 6994 Intron NP_055504.2
XM_005246673.4 6994 Intron XP_005246730.1
XM_006712617.3 6994 Intron XP_006712680.1
XM_017004441.1 6994 Missense Mutation AAT,CAT N,H 2240 XP_016859930.1
XM_017004442.1 6994 Missense Mutation AAT,CAT N,H 2231 XP_016859931.1
XM_017004443.1 6994 Missense Mutation AAT,CAT N,H 2227 XP_016859932.1
XM_017004444.1 6994 Missense Mutation AAT,CAT N,H 2225 XP_016859933.1
XM_017004445.1 6994 Missense Mutation AAT,CAT N,H 2221 XP_016859934.1
XM_017004446.1 6994 Missense Mutation AAT,CAT N,H 2191 XP_016859935.1
XM_017004447.1 6994 Intron XP_016859936.1

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