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CTTGTACACCACATGTGGTCCACTT[C/T]CCTCCGGGCTCCGAGAACCCTTGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608990 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ADAMTS10 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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ADAMTS10 - ADAM metallopeptidase with thrombospondin type 1 motif 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282352.1 | 824 | Intron | NP_001269281.1 | |||
NM_030957.3 | 824 | Missense Mutation | GAA,GGA | E,G 173 | NP_112219.3 | |
XM_006722917.3 | 824 | UTR 5 | XP_006722980.1 | |||
XM_017027338.1 | 824 | Missense Mutation | GAA,GGA | E,G 173 | XP_016882827.1 | |
XM_017027339.1 | 824 | Intron | XP_016882828.1 | |||
XM_017027340.1 | 824 | Intron | XP_016882829.1 |