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GCCTGTGTGAGCCGAGGTGGCCGCT[A/G]GCTGGAGATTGGTTTGCACTTCTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608937 MIM: 602389 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SH2B1 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SH2B1 - SH2B adaptor protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145795.1 | 466 | Intron | NP_001139267.1 | |||
NM_001145796.1 | 466 | Intron | NP_001139268.1 | |||
NM_001145797.1 | 466 | Intron | NP_001139269.1 | |||
NM_001145812.1 | 466 | Intron | NP_001139284.1 | |||
NM_001308293.1 | 466 | Intron | NP_001295222.1 | |||
NM_001308294.1 | 466 | Intron | NP_001295223.1 | |||
NM_015503.2 | 466 | UTR 5 | NP_056318.2 | |||
XM_017023114.1 | 466 | Intron | XP_016878603.1 | |||
XM_017023115.1 | 466 | Intron | XP_016878604.1 | |||
XM_017023116.1 | 466 | UTR 5 | XP_016878605.1 | |||
XM_017023117.1 | 466 | Intron | XP_016878606.1 | |||
XM_017023118.1 | 466 | Intron | XP_016878607.1 | |||
XM_017023119.1 | 466 | Intron | XP_016878608.1 | |||
XM_017023120.1 | 466 | Intron | XP_016878609.1 |
TUFM - Tu translation elongation factor, mitochondrial | ||||||
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There are no transcripts associated with this gene. |