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AAGGGTCTCCCAGGTATGTGACCCA[A/G]GAGCCTCAGCCCTCGAGGAGACAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608349 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
HSH2D PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
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Caucasian
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CEPH (CEU) - Not Available | ||||||
EAS
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African American
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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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HSH2D - hematopoietic SH2 domain containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291274.1 | Intron | NP_001278203.1 | ||||
NM_032855.3 | Intron | NP_116244.1 | ||||
XM_011528386.2 | Intron | XP_011526688.1 | ||||
XM_011528387.2 | Intron | XP_011526689.1 | ||||
XM_011528388.2 | Intron | XP_011526690.1 | ||||
XM_011528389.2 | Intron | XP_011526691.1 | ||||
XM_011528390.1 | Intron | XP_011526692.1 | ||||
XM_017027402.1 | Intron | XP_016882891.1 | ||||
XM_017027403.1 | Intron | XP_016882892.1 | ||||
XM_017027404.1 | Intron | XP_016882893.1 |
Set Membership: |
Validated |