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TACTGATGCAGGCACTGCAGGAGCC[C/T]TGACTCCACAGCATGTTCGAGCTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606608 | ||||||||||||||||||||
Literature Links: |
YAP1 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 |
YAP1 - Yes associated protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130145.2 | 740 | Silent Mutation | CTG,TTG | L,L 118 | NP_001123617.1 | |
NM_001195044.1 | 740 | Silent Mutation | CTG,TTG | L,L 118 | NP_001181973.1 | |
NM_001195045.1 | 740 | UTR 5 | NP_001181974.1 | |||
NM_001282097.1 | 740 | Silent Mutation | CTG,TTG | L,L 118 | NP_001269026.1 | |
NM_001282098.1 | 740 | Silent Mutation | CTG,TTG | L,L 118 | NP_001269027.1 | |
NM_001282099.1 | 740 | Silent Mutation | CTG,TTG | L,L 118 | NP_001269028.1 | |
NM_001282100.1 | 740 | Silent Mutation | CTG,TTG | L,L 118 | NP_001269029.1 | |
NM_001282101.1 | 740 | Silent Mutation | CTG,TTG | L,L 118 | NP_001269030.1 | |
NM_006106.4 | 740 | Silent Mutation | CTG,TTG | L,L 118 | NP_006097.2 | |
XM_005271378.3 | 740 | Silent Mutation | CTG,TTG | L,L 118 | XP_005271435.1 | |
XM_005271380.3 | 740 | Silent Mutation | CTG,TTG | L,L 118 | XP_005271437.1 | |
XM_005271381.3 | 740 | Silent Mutation | CTG,TTG | L,L 118 | XP_005271438.1 | |
XM_005271383.3 | 740 | Silent Mutation | CTG,TTG | L,L 118 | XP_005271440.1 | |
XM_011542555.2 | 740 | UTR 5 | XP_011540857.1 | |||
XM_011542556.2 | 740 | UTR 5 | XP_011540858.1 | |||
XM_017017093.1 | 740 | UTR 5 | XP_016872582.1 |