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See other ARL5C GT Assays ›
SNP ID:
rs529955
Gene
ARL5C CACNB1
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.17: 39175783 - 39175783 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

TGGATGAAGAGGGTGCTGGCTCTAG[A/G]GGAGGGGCCCCGGGGACAAACGGCT

Assay ID C____525960_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: 114207

Literature Links:

 ARL5C PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.32)
(0.68)
Caucasian - Not Available CEPH (CEU)
G (0.24)
(0.76)
EAS
G (0.25)
(0.75)
African American - Not Available YRI (Yoruba)
A (0.34)
(0.66)
SAS
G (0.14)
(0.86)
Chinese - Not Available JPT (Japanese)
G (0.16)
(0.84)
AFR
A (0.36)
(0.64)
Japanese - Not Available CHB (Han Chinese)
G (0.28)
(0.72)
EUR
G (0.23)
(0.77)
AMR
G (0.19)
(0.81)
ARL5C - ADP ribosylation factor like GTPase 5C
There are no transcripts associated with this gene.
CACNB1 - calcium voltage-gated channel auxiliary subunit beta 1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_000723.4 Intron NP_000714.3
NM_199247.2 Intron NP_954855.1
NM_199248.2 Intron NP_954856.1
XM_005257645.2 Intron XP_005257702.1
XM_005257646.2 Intron XP_005257703.1
XM_006722072.2 Intron XP_006722135.1
XM_017025024.1 Intron XP_016880513.1
XM_017025025.1 Intron XP_016880514.1
XM_017025026.1 Intron XP_016880515.1
XM_017025027.1 Intron XP_016880516.1
XM_017025028.1 Intron XP_016880517.1
XM_017025029.1 Intron XP_016880518.1
XM_017025030.1 Intron XP_016880519.1

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