Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTGACTTCGAAAACTGTGGCTGTG[G/A]TGGGTCAAACAATGGAAAAACAGGT
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 |
---|---|---|
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 |
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 | 612 | Missense Mutation | GAT,GGT | D,G 133 | NP_001287867.1 | |
NM_001300939.1 | 612 | Missense Mutation | GAT,GGT | D,G 133 | NP_001287868.1 | |
NM_058244.3 | 612 | Missense Mutation | GAT,GGT | D,G 115 | NP_490645.1 | |
XM_011543625.2 | 612 | Missense Mutation | GAT,GGT | D,G 155 | XP_011541927.2 | |
XM_017009824.1 | 612 | Missense Mutation | GAT,GGT | D,G 155 | XP_016865313.1 | |
XM_017009825.1 | 612 | Missense Mutation | GAT,GGT | D,G 155 | XP_016865314.1 | |
XM_017009826.1 | 612 | Missense Mutation | GAT,GGT | D,G 19 | XP_016865315.1 |