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TGGCAGCTTCGGGGGCCGCCACAGC[A/G]TATTTCAGCTCCTTCAGTGCCTATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 114220 MIM: 611696 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CAPN1 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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CAPN1 - calpain 1 | ||||||
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There are no transcripts associated with this gene. |
SLC22A20 - solute carrier family 22 member 20 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001004326.4 | 585 | Silent Mutation | GCA,GCG | A,A 184 | NP_001004326.4 | |
XM_011545043.2 | 585 | Silent Mutation | GCA,GCG | A,A 184 | XP_011543345.1 | |
XM_017017774.1 | 585 | Silent Mutation | GCA,GCG | A,A 184 | XP_016873263.1 | |
XM_017017775.1 | 585 | Intron | XP_016873264.1 | |||
XM_017017776.1 | 585 | Intron | XP_016873265.1 |