Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCTTGGTATGCTTGTTGTGACTGAT[C/T]GACAATCCCTGGATAAGACACACCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601288 | ||||||||||||||||||||
Literature Links: |
YWHAZ 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 |
YWHAZ - tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135699.1 | 962 | Intron | NP_001129171.1 | |||
NM_001135700.1 | 962 | Intron | NP_001129172.1 | |||
NM_001135701.1 | 962 | Intron | NP_001129173.1 | |||
NM_001135702.1 | 962 | Intron | NP_001129174.1 | |||
NM_003406.3 | 962 | Intron | NP_003397.1 | |||
NM_145690.2 | 962 | Intron | NP_663723.1 | |||
XM_005251061.3 | 962 | Missense Mutation | AAT,GAT | N,D 143 | XP_005251118.1 | |
XM_005251063.3 | 962 | Missense Mutation | AAT,GAT | N,D 143 | XP_005251120.1 | |
XM_011517290.2 | 962 | Intron | XP_011515592.1 | |||
XM_017013810.1 | 962 | Missense Mutation | AAT,GAT | N,D 143 | XP_016869299.1 | |
XM_017013811.1 | 962 | Missense Mutation | AAT,GAT | N,D 143 | XP_016869300.1 | |
XM_017013812.1 | 962 | Intron | XP_016869301.1 |