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GCTGGAACTGCCCTGAAAATGCTCT[G/T]CAGCTCTCCACCCACAACAGGCTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606360 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
WNT8A PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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WNT8A - Wnt family member 8A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300938.1 | 478 | Silent Mutation | CTG,CTT | L,L 88 | NP_001287867.1 | |
NM_001300939.1 | 478 | Silent Mutation | CTG,CTT | L,L 88 | NP_001287868.1 | |
NM_058244.3 | 478 | Silent Mutation | CTG,CTT | L,L 70 | NP_490645.1 | |
XM_011543625.2 | 478 | Silent Mutation | CTG,CTT | L,L 110 | XP_011541927.2 | |
XM_017009824.1 | 478 | Silent Mutation | CTG,CTT | L,L 110 | XP_016865313.1 | |
XM_017009825.1 | 478 | Silent Mutation | CTG,CTT | L,L 110 | XP_016865314.1 | |
XM_017009826.1 | 478 | UTR 5 | XP_016865315.1 |