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CCAGCTCCCCTGGGTACTCGTGCAT[A/G]CTGGCGTGCTCCCCGGTGGCCCGTT
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | 1959 | Silent Mutation | AGC,AGT | S,S 464 | NP_000714.3 | |
NM_199247.2 | 1959 | Intron | NP_954855.1 | |||
NM_199248.2 | 1959 | Intron | NP_954856.1 | |||
XM_005257645.2 | 1959 | Silent Mutation | AGC,AGT | S,S 509 | XP_005257702.1 | |
XM_005257646.2 | 1959 | Intron | XP_005257703.1 | |||
XM_006722072.2 | 1959 | Silent Mutation | AGC,AGT | S,S 462 | XP_006722135.1 | |
XM_017025024.1 | 1959 | Silent Mutation | AGC,AGT | S,S 465 | XP_016880513.1 | |
XM_017025025.1 | 1959 | Silent Mutation | AGC,AGT | S,S 417 | XP_016880514.1 | |
XM_017025026.1 | 1959 | Silent Mutation | AGC,AGT | S,S 297 | XP_016880515.1 | |
XM_017025027.1 | 1959 | Silent Mutation | AGC,AGT | S,S 236 | XP_016880516.1 | |
XM_017025028.1 | 1959 | Silent Mutation | AGC,AGT | S,S 236 | XP_016880517.1 | |
XM_017025029.1 | 1959 | Silent Mutation | AGC,AGT | S,S 236 | XP_016880518.1 | |
XM_017025030.1 | 1959 | Intron | XP_016880519.1 |