Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGTCCCTTGGCTTGCTTCCCCAGG[A/T]TGGCACAGTGTTCGACAGCCGCCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 400033 | ||||||||||||||||||||
Literature Links: |
TBL1Y 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 |
TBL1Y - transducin (beta)-like 1, Y-linked | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033284.1 | 758 | Missense Mutation | GAT,GTT | D,V 69 | NP_150600.1 | |
NM_134258.1 | 758 | Missense Mutation | GAT,GTT | D,V 69 | NP_599020.1 | |
NM_134259.1 | 758 | Missense Mutation | GAT,GTT | D,V 69 | NP_599021.1 | |
XM_005262572.3 | 758 | Missense Mutation | GAT,GTT | D,V 83 | XP_005262629.1 | |
XM_017030086.1 | 758 | Missense Mutation | GAT,GTT | D,V 69 | XP_016885575.1 | |
XM_017030087.1 | 758 | Missense Mutation | GAT,GTT | D,V 69 | XP_016885576.1 |