Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTACACACATACCTGGCGCCCCAC[C/T]CTGTTGTTGTGGATTCGCATTCGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601906 | ||||||||||||||||||||
Literature Links: |
WNT10B 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 |
WNT10B - Wnt family member 10B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003394.3 | 541 | Silent Mutation | AGA,AGG | R,R 233 | NP_003385.2 | |
XM_011538722.1 | 541 | Silent Mutation | AGA,AGG | R,R 111 | XP_011537024.1 | |
XM_011538724.1 | 541 | Missense Mutation | AGT,GGT | S,G 158 | XP_011537026.1 | |
XM_017019919.1 | 541 | Silent Mutation | AGA,AGG | R,R 111 | XP_016875408.1 |