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CTGCAGGGTCTCCAAGCCCTGGCCC[C/T]TCTGAGGGGTCAGTCTCCATGTCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 114207 | ||||||||||||||||||||
Literature Links: |
ARL5C PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ARL5C - ADP ribosylation factor like GTPase 5C | ||||||
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There are no transcripts associated with this gene. |
CACNB1 - calcium voltage-gated channel auxiliary subunit beta 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000723.4 | 2151 | Silent Mutation | GAA,GAG | E,E 528 | NP_000714.3 | |
NM_199247.2 | 2151 | Intron | NP_954855.1 | |||
NM_199248.2 | 2151 | Intron | NP_954856.1 | |||
XM_005257645.2 | 2151 | Silent Mutation | GAA,GAG | E,E 573 | XP_005257702.1 | |
XM_005257646.2 | 2151 | Intron | XP_005257703.1 | |||
XM_006722072.2 | 2151 | Silent Mutation | GAA,GAG | E,E 526 | XP_006722135.1 | |
XM_017025024.1 | 2151 | Silent Mutation | GAA,GAG | E,E 529 | XP_016880513.1 | |
XM_017025025.1 | 2151 | Silent Mutation | GAA,GAG | E,E 481 | XP_016880514.1 | |
XM_017025026.1 | 2151 | Silent Mutation | GAA,GAG | E,E 361 | XP_016880515.1 | |
XM_017025027.1 | 2151 | Silent Mutation | GAA,GAG | E,E 300 | XP_016880516.1 | |
XM_017025028.1 | 2151 | Silent Mutation | GAA,GAG | E,E 300 | XP_016880517.1 | |
XM_017025029.1 | 2151 | Silent Mutation | GAA,GAG | E,E 300 | XP_016880518.1 | |
XM_017025030.1 | 2151 | Intron | XP_016880519.1 |