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SNP ID:
rs8344
Gene
CNST
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.1: 246668054 - 246668054 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

CGCCACTTCCCAGGGAGGGTGAGGT[A/G]AGCTCGGGAACATAACGATGTTTTG

Assay ID C___7482581_30
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 38 submissions

Phenotype:

 MIM: 613439

Literature Links:

 CNST PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.18)
(0.82)
Caucasian - Not Available CEPH (CEU)
T (0.22)
(0.78)
EAS
T (0.13)
(0.87)
African American - Not Available YRI (Yoruba)
T (0.13)
(0.87)
SAS
T (0.22)
(0.78)
Chinese - Not Available JPT (Japanese)
T (0.20)
(0.80)
AFR
T (0.12)
(0.88)
Japanese - Not Available CHB (Han Chinese)
T (0.11)
(0.89)
EUR
T (0.23)
(0.77)
AMR
T (0.22)
(0.78)
CNST - consortin, connexin sorting protein
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001139459.1 4274 Intron NP_001132931.1
NM_152609.2 4274 UTR 3 NP_689822.2
XM_005273081.3 4274 UTR 3 XP_005273138.2
XM_005273083.4 4274 UTR 3 XP_005273140.1
XM_011544110.2 4274 UTR 3 XP_011542412.1
XM_011544111.1 4274 UTR 3 XP_011542413.1
XM_011544112.1 4274 UTR 3 XP_011542414.1
XM_011544113.1 4274 UTR 3 XP_011542415.1
XM_011544114.2 4274 UTR 3 XP_011542416.1
XM_017000487.1 4274 UTR 3 XP_016855976.1
XM_017000488.1 4274 UTR 3 XP_016855977.1
XM_017000489.1 4274 UTR 3 XP_016855978.1

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