Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606032 MIM: 600787 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SRRM2 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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SRRM2 - serine/arginine repetitive matrix 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016333.3 | 880 | Intron | NP_057417.3 | |||
XM_005255226.1 | 880 | Intron | XP_005255283.1 | |||
XM_006720874.3 | 880 | Intron | XP_006720937.1 |
TCEB2 - transcription elongation factor B subunit 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_007108.3 | 880 | UTR 3 | NP_009039.1 | |||
NM_207013.2 | 880 | Missense Mutation | ACG,ATG | T,M 145 | NP_996896.1 |
Set Membership: |
HapMap |