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Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603267 MIM: 605754 | ||||||||||||||||||||
Literature Links: |
CAPN15 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
CAPN15 - calpain 15 | ||||||
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There are no transcripts associated with this gene. |
LOC107987233 - uncharacterized LOC107987233 | ||||||
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There are no transcripts associated with this gene. |
NHLRC4 - NHL repeat containing 4 | ||||||
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There are no transcripts associated with this gene. |
PIGQ - phosphatidylinositol glycan anchor biosynthesis class Q | ||||||
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There are no transcripts associated with this gene. |
PRR35 - proline rich 35 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_145270.2 | 1013 | Missense Mutation | CCG,CTG | P,L 245 | NP_660313.1 | |
XM_017022959.1 | 1013 | Missense Mutation | CCG,CTG | P,L 245 | XP_016878448.1 | |
XM_017022960.1 | 1013 | Missense Mutation | CCG,CTG | P,L 245 | XP_016878449.1 | |
XM_017022961.1 | 1013 | Intron | XP_016878450.1 |