Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGCGGCACAACAGCCTGGCAGGGG[C/T]GCCCGAGCCAGGCAGGACGCTGCCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
28 submissions
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 603876 MIM: 602985 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ADAMTS4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
ADAMTS4 - ADAM metallopeptidase with thrombospondin type 1 motif 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320336.1 | 655 | Missense Mutation | ACC,GCC | T,A 77 | NP_001307265.1 | |
NM_005099.5 | 655 | Missense Mutation | ACC,GCC | T,A 77 | NP_005090.3 |
NDUFS2 - NADH:ubiquinone oxidoreductase core subunit S2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166159.1 | 655 | Intron | NP_001159631.1 | |||
NM_004550.4 | 655 | Intron | NP_004541.1 | |||
XM_005245208.2 | 655 | Intron | XP_005245265.1 | |||
XM_005245209.1 | 655 | Intron | XP_005245266.1 | |||
XM_017001357.1 | 655 | Intron | XP_016856846.1 |