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Search Thermo Fisher Scientific
CCGGGGGCTGGAATGGGGGAGGCAT[C/T]TGGGGGTGGGGTGGGCACAGGGCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613479 | ||||||||||||||||||||
Literature Links: |
CEP131 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 |
CEP131 - centrosomal protein 131 | ||||||
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There are no transcripts associated with this gene. |
LOC105371925 - uncharacterized LOC105371925 | ||||||
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There are no transcripts associated with this gene. |
TEPSIN - TEPSIN, adaptor related protein complex 4 accessory protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144679.2 | 2564 | Missense Mutation | AAT,GAT | N,D 421 | NP_653280.1 | |
XM_005257066.2 | 2564 | Missense Mutation | AAT,GAT | N,D 699 | XP_005257123.1 | |
XM_005257067.2 | 2564 | Missense Mutation | AAT,GAT | N,D 489 | XP_005257124.1 | |
XM_006721709.3 | 2564 | Missense Mutation | AAT,GAT | N,D 491 | XP_006721772.1 | |
XM_006721712.2 | 2564 | Missense Mutation | AAT,GAT | N,D 337 | XP_006721775.1 | |
XM_011524355.1 | 2564 | Missense Mutation | AAT,GAT | N,D 701 | XP_011522657.1 | |
XM_011524356.1 | 2564 | Missense Mutation | AAT,GAT | N,D 633 | XP_011522658.1 | |
XM_011524357.1 | 2564 | Missense Mutation | AAT,GAT | N,D 484 | XP_011522659.1 | |
XM_011524358.2 | 2564 | Missense Mutation | AAT,GAT | N,D 484 | XP_011522660.1 | |
XM_017024202.1 | 2564 | Missense Mutation | AAT,GAT | N,D 532 | XP_016879691.1 | |
XM_017024203.1 | 2564 | Missense Mutation | AAT,GAT | N,D 511 | XP_016879692.1 | |
XM_017024204.1 | 2564 | Missense Mutation | AAT,GAT | N,D 484 | XP_016879693.1 |