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AGGTGTTTCACTCTGAAAAAGAGAC[A/G]AAGAGCTCAAGAATAAAGGCTGAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604445 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SERPINB13 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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SERPINB13 - serpin family B member 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001307923.1 | 357 | Silent Mutation | ACA,ACG | T,T 63 | NP_001294852.1 | |
NM_012397.3 | 357 | Silent Mutation | ACA,ACG | T,T 63 | NP_036529.1 | |
XM_005266707.3 | 357 | UTR 5 | XP_005266764.1 | |||
XM_011526029.2 | 357 | Silent Mutation | ACA,ACG | T,T 63 | XP_011524331.1 |