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SNP ID:
rs906220
Gene
HK1
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.10: 69300854 - 69300854 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

GGAAAGATGGCAAAAAGAGCCCTGC[A/G]TGATTTTGTACGTAGAAAATCCTGG

Assay ID C___8863428_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 142600

Literature Links:

 HK1 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.09)
(0.91)
Caucasian - Not Available CEPH (CEU)
A (0.06)
(0.94)
EAS
A (0.01)
(0.99)
African American - Not Available YRI (Yoruba)
A (0.22)
(0.78)
SAS
A (0.11)
(0.89)
Chinese - Not Available CHB (Han Chinese)
A (0.01)
(0.99)
AFR
A (0.17)
(0.83)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
A (0.07)
(0.93)
AMR
A (0.09)
(0.91)
HK1 - hexokinase 1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_000188.2 519 Intron NP_000179.2
NM_001322364.1 519 Intron NP_001309293.1
NM_001322365.1 519 Intron NP_001309294.1
NM_001322366.1 519 Intron NP_001309295.1
NM_001322367.1 519 Intron NP_001309296.1
NM_033496.2 519 Intron NP_277031.1
NM_033497.2 519 Intron NP_277032.1
NM_033498.2 519 Intron NP_277033.1
NM_033500.2 519 Missense Mutation CAT,CGT H,R 7 NP_277035.2
XM_005269737.1 519 Intron XP_005269794.1
XM_011539732.1 519 Missense Mutation CAT,CGT H,R 7 XP_011538034.1

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