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GGCTGTTGGGAGACAGCTTGGACTC[C/T]GTTTCATGCAGGGCTGGTTTAGATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610228 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CAPN13 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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CAPN13 - calpain 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144575.2 | 2507 | UTR 3 | NP_653176.2 | |||
XM_011533159.2 | 2507 | Intron | XP_011531461.1 | |||
XM_011533160.2 | 2507 | Intron | XP_011531462.1 | |||
XM_011533161.2 | 2507 | Intron | XP_011531463.1 | |||
XM_011533163.2 | 2507 | Intron | XP_011531465.1 | |||
XM_017005264.1 | 2507 | UTR 3 | XP_016860753.1 | |||
XM_017005265.1 | 2507 | Intron | XP_016860754.1 | |||
XM_017005266.1 | 2507 | Intron | XP_016860755.1 |