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CAGGTTGCATTTCCCAGTATTTCAC[C/T]GGGTTGTTGAATAAACTTATTGCAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608135 MIM: 611505 | ||||||||||||||||||||
Literature Links: |
ASPN PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
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 |
ASPN - asporin | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193335.1 | 1123 | UTR 3 | NP_001180264.1 | |||
NM_017680.4 | 1123 | Silent Mutation | CCA,CCG | P,P 352 | NP_060150.4 |
CENPP - centromere protein P | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012267.2 | 1123 | Intron | NP_001012267.1 | |||
NM_001286969.1 | 1123 | Intron | NP_001273898.1 | |||
NM_001286971.1 | 1123 | Intron | NP_001273900.1 | |||
XM_011518685.2 | 1123 | Intron | XP_011516987.1 | |||
XM_011518689.1 | 1123 | Intron | XP_011516991.1 | |||
XM_017014715.1 | 1123 | Intron | XP_016870204.1 |