Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GACAGTTCGCATTCGGAGAAAAAGA[C/T]GGCGAAGAGGAAGGGCTCGGCTGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 605925 | ||||||||||||||||||||
Literature Links: |
C21orf58 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
C21orf58 - chromosome 21 open reading frame 58 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
PCNT - pericentrin | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001315529.1 | 408 | UTR 5 | NP_001302458.1 | |||
NM_006031.5 | 408 | Missense Mutation | ACG,ATG | T,M 38 | NP_006022.3 | |
XM_005261124.4 | 408 | Missense Mutation | ACG,ATG | T,M 38 | XP_005261181.1 | |
XM_011529594.2 | 408 | Missense Mutation | ACG,ATG | T,M 38 | XP_011527896.1 | |
XM_017028362.1 | 408 | Missense Mutation | ACG,ATG | T,M 38 | XP_016883851.1 | |
XM_017028363.1 | 408 | UTR 5 | XP_016883852.1 |