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See other CRYZ GT Assays ›
SNP ID:
rs17459
Gene
CRYZ
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.1: 74706067 - 74706067 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

CTCATGCCAAATGACAACTAACATG[C/T]TATTTCCTACTATGATGACTCTTTG

Assay ID C___8909141_20
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 62 submissions

Phenotype:

 MIM: 123691

Literature Links:

 CRYZ PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.39)
(0.61)
Caucasian - Not Available CEPH (CEU)
T (0.34)
(0.66)
EAS
T (0.31)
(0.69)
African American - Not Available YRI (Yoruba)
C (0.49)
(0.51)
SAS
T (0.44)
(0.56)
Chinese - Not Available JPT (Japanese)
T (0.25)
(0.75)
AFR
T (0.49)
(0.51)
Japanese - Not Available CHB (Han Chinese)
T (0.30)
(0.70)
EUR
T (0.40)
(0.60)
AMR
T (0.28)
(0.72)
CRYZ - crystallin zeta
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001130042.1 1208 UTR 3 NP_001123514.1
NM_001130043.1 1208 UTR 3 NP_001123515.1
NM_001134759.1 1208 UTR 3 NP_001128231.1
NM_001889.3 1208 UTR 3 NP_001880.2
XM_005270491.4 1208 UTR 3 XP_005270548.1
XM_011540747.1 1208 UTR 3 XP_011539049.1
XM_017000367.1 1208 UTR 3 XP_016855856.1
XM_017000368.1 1208 UTR 3 XP_016855857.1

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