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GCTGTAAAACGTGCTGCACAGCCTT[A/G]ACCCCAAAGGAAAAGCAACCCTTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 118425 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CLCN1 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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CLCN1 - chloride voltage-gated channel 1 | ||||||
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There are no transcripts associated with this gene. |
FAM131B - family with sequence similarity 131 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031690.2 | 3796 | UTR 3 | NP_001026860.2 | |||
NM_001278297.1 | 3796 | UTR 3 | NP_001265226.1 | |||
NM_014690.4 | 3796 | UTR 3 | NP_055505.3 | |||
XM_005250073.3 | 3796 | UTR 3 | XP_005250130.1 | |||
XM_006716186.2 | 3796 | UTR 3 | XP_006716249.1 |