Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCAGATGAGACTCCCATGTTGCCCC[A/G]CTGATCTCTGGTCACTCCCAGGAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604721 MIM: 604504 | ||||||||||||||||||||
Literature Links: |
SH2D3A 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 |
SH2D3A - SH2 domain containing 3A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005490.2 | 776 | Missense Mutation | CGG,TGG | R,W 339 | NP_005481.2 | |
XM_005259467.1 | 776 | Missense Mutation | CGG,TGG | R,W 339 | XP_005259524.1 | |
XM_005259472.2 | 776 | Missense Mutation | CGG,TGG | R,W 217 | XP_005259529.1 | |
XM_006722602.1 | 776 | Missense Mutation | GCG,GTG | A,V 211 | XP_006722665.1 | |
XM_011527608.2 | 776 | Missense Mutation | CGG,TGG | R,W 244 | XP_011525910.1 | |
XM_011527609.2 | 776 | Missense Mutation | CGG,TGG | R,W 244 | XP_011525911.1 | |
XM_017026123.1 | 776 | Missense Mutation | CGG,TGG | R,W 339 | XP_016881612.1 | |
XM_017026124.1 | 776 | Missense Mutation | GCG,GTG | A,V 211 | XP_016881613.1 |
TRIP10 - thyroid hormone receptor interactor 10 | ||||||
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There are no transcripts associated with this gene. |