Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCACAGGGATGCCATAAAGAGGATC[A/G]ACCAGTCAGAGTTCGAAGGCTTTGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
|
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Phenotype: |
MIM: 615183 MIM: 176982 | ||||||||||||||||||||
Literature Links: |
FAAP20 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 |
FAAP20 - Fanconi anemia core complex associated protein 20 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146310.1 | 1780 | UTR 3 | NP_001139782.1 | |||
NM_001256945.1 | 1780 | UTR 3 | NP_001243874.1 | |||
NM_001256946.1 | 1780 | Intron | NP_001243875.1 | |||
NM_001256947.1 | 1780 | Intron | NP_001243876.1 | |||
NM_001282670.1 | 1780 | Intron | NP_001269599.1 | |||
NM_001282671.1 | 1780 | UTR 3 | NP_001269600.1 | |||
NM_001282672.1 | 1780 | UTR 3 | NP_001269601.1 | |||
NM_001282673.1 | 1780 | UTR 3 | NP_001269602.1 | |||
NM_182533.2 | 1780 | Intron | NP_872339.2 | |||
XM_006710419.3 | 1780 | Intron | XP_006710482.1 | |||
XM_006710421.3 | 1780 | Intron | XP_006710484.1 | |||
XM_011540914.2 | 1780 | Intron | XP_011539216.1 | |||
XM_011540921.2 | 1780 | Intron | XP_011539223.1 | |||
XM_011540922.1 | 1780 | Intron | XP_011539224.1 | |||
XM_017000553.1 | 1780 | Intron | XP_016856042.1 | |||
XM_017000554.1 | 1780 | UTR 3 | XP_016856043.1 | |||
XM_017000555.1 | 1780 | Intron | XP_016856044.1 | |||
XM_017000556.1 | 1780 | Intron | XP_016856045.1 | |||
XM_017000557.1 | 1780 | Intron | XP_016856046.1 |
LOC100506504 - uncharacterized LOC100506504 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_011542503.2 | 1780 | Intron | XP_011540805.1 |
PRKCZ - protein kinase C zeta | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033581.1 | 1780 | Missense Mutation | AAC,GAC | N,D 388 | NP_001028753.1 | |
NM_001033582.1 | 1780 | Missense Mutation | AAC,GAC | N,D 388 | NP_001028754.1 | |
NM_001242874.1 | 1780 | Missense Mutation | AAC,GAC | N,D 467 | NP_001229803.1 | |
NM_002744.4 | 1780 | Missense Mutation | AAC,GAC | N,D 571 | NP_002735.3 | |
XM_011541773.1 | 1780 | Intron | XP_011540075.1 | |||
XM_011541774.1 | 1780 | Intron | XP_011540076.1 | |||
XM_011541775.2 | 1780 | Intron | XP_011540077.1 | |||
XM_011541776.1 | 1780 | Intron | XP_011540078.1 | |||
XM_011541778.1 | 1780 | Intron | XP_011540080.1 | |||
XM_017001789.1 | 1780 | Intron | XP_016857278.1 | |||
XM_017001790.1 | 1780 | Missense Mutation | AAC,GAC | N,D 579 | XP_016857279.1 | |
XM_017001791.1 | 1780 | Missense Mutation | AAC,GAC | N,D 489 | XP_016857280.1 | |
XM_017001792.1 | 1780 | Intron | XP_016857281.1 | |||
XM_017001793.1 | 1780 | Intron | XP_016857282.1 | |||
XM_017001794.1 | 1780 | Intron | XP_016857283.1 | |||
XM_017001795.1 | 1780 | Intron | XP_016857284.1 | |||
XM_017001796.1 | 1780 | Missense Mutation | AAC,GAC | N,D 396 | XP_016857285.1 | |
XM_017001797.1 | 1780 | Intron | XP_016857286.1 | |||
XM_017001798.1 | 1780 | Missense Mutation | AAC,GAC | N,D 396 | XP_016857287.1 | |
XM_017001799.1 | 1780 | Missense Mutation | AAC,GAC | N,D 388 | XP_016857288.1 | |
XM_017001800.1 | 1780 | Intron | XP_016857289.1 | |||
XM_017001801.1 | 1780 | Missense Mutation | AAC,GAC | N,D 384 | XP_016857290.1 | |
XM_017001802.1 | 1780 | Intron | XP_016857291.1 | |||
XM_017001803.1 | 1780 | Intron | XP_016857292.1 | |||
XM_017001804.1 | 1780 | Missense Mutation | AAC,GAC | N,D 334 | XP_016857293.1 | |
XM_017001805.1 | 1780 | Missense Mutation | AAC,GAC | N,D 334 | XP_016857294.1 |