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GGTTTCTGGAATAGTTTAGGGGAGA[A/G]ATGGTAAGGGTCTGAGCAGAAGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 300008 | ||||||||||||||||||||
Literature Links: |
CLCN5 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 |
CLCN5 - chloride voltage-gated channel 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000084.4 | Intron | NP_000075.1 | ||||
NM_001127898.3 | Intron | NP_001121370.1 | ||||
NM_001127899.3 | Intron | NP_001121371.1 | ||||
NM_001272102.1 | Intron | NP_001259031.1 | ||||
NM_001282163.1 | Intron | NP_001269092.1 | ||||
XM_017029257.1 | Intron | XP_016884746.1 | ||||
XM_017029258.1 | Intron | XP_016884747.1 |