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GAATGGCTGTCATAGTAACCAGACC[A/G]GAAACAATGGTGCTTGGACTAAAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606503 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SUV39H2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
SUV39H2 - suppressor of variegation 3-9 homolog 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193424.1 | Intron | NP_001180353.1 | ||||
NM_001193425.1 | Intron | NP_001180354.1 | ||||
NM_001193426.1 | Intron | NP_001180355.1 | ||||
NM_001193427.1 | Intron | NP_001180356.1 | ||||
NM_024670.3 | Intron | NP_078946.1 | ||||
XM_006717503.3 | Intron | XP_006717566.1 | ||||
XM_011519662.2 | Intron | XP_011517964.1 | ||||
XM_017016637.1 | Intron | XP_016872126.1 |