Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604722 MIM: 608052 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SH2D3C 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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SH2D3C - SH2 domain containing 3C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142531.1 | 1735 | Silent Mutation | GCC,GCT | A,A 341 | NP_001136003.1 | |
NM_001142532.1 | 1735 | Silent Mutation | GCC,GCT | A,A 341 | NP_001136004.1 | |
NM_001142533.1 | 1735 | Silent Mutation | GCC,GCT | A,A 537 | NP_001136005.1 | |
NM_001142534.1 | 1735 | Silent Mutation | GCC,GCT | A,A 535 | NP_001136006.1 | |
NM_001252334.1 | 1735 | Silent Mutation | GCC,GCT | A,A 627 | NP_001239263.1 | |
NM_005489.3 | 1735 | Silent Mutation | GCC,GCT | A,A 538 | NP_005480.2 | |
NM_170600.2 | 1735 | Silent Mutation | GCC,GCT | A,A 695 | NP_733745.1 | |
XM_005251639.1 | 1735 | Silent Mutation | GCC,GCT | A,A 341 | XP_005251696.1 | |
XM_011518114.1 | 1735 | Silent Mutation | GCC,GCT | A,A 639 | XP_011516416.1 | |
XM_011518115.1 | 1735 | Silent Mutation | GCC,GCT | A,A 639 | XP_011516417.1 | |
XM_011518117.2 | 1735 | Silent Mutation | GCC,GCT | A,A 341 | XP_011516419.1 | |
XM_017014174.1 | 1735 | Silent Mutation | GCC,GCT | A,A 341 | XP_016869663.1 |
TOR2A - torsin family 2 member A | ||||||
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There are no transcripts associated with this gene. |