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ACCAGCACCGGATGCTGAGCTGGCC[A/G]CACAGGCAGTTGGAGCTAGAGCAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604599 MIM: 606107 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EHMT2 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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EHMT2 - euchromatic histone lysine methyltransferase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289413.1 | 3055 | Silent Mutation | TGC,TGT | C,C 1010 | NP_001276342.1 | |
NM_001318833.1 | 3055 | Silent Mutation | TGC,TGT | C,C 785 | NP_001305762.1 | |
NM_006709.4 | 3055 | Silent Mutation | TGC,TGT | C,C 987 | NP_006700.3 | |
NM_025256.6 | 3055 | Silent Mutation | TGC,TGT | C,C 953 | NP_079532.5 | |
XM_005248824.3 | 3055 | Silent Mutation | TGC,TGT | C,C 1044 | XP_005248881.1 | |
XM_006714974.1 | 3055 | Silent Mutation | TGC,TGT | C,C 1051 | XP_006715037.1 | |
XM_006714975.1 | 3055 | Silent Mutation | TGC,TGT | C,C 1017 | XP_006715038.1 | |
XM_006714976.1 | 3055 | Silent Mutation | TGC,TGT | C,C 994 | XP_006715039.1 | |
XM_017010202.1 | 3055 | Silent Mutation | TGC,TGT | C,C 960 | XP_016865691.1 |
SLC44A4 - solute carrier family 44 member 4 | ||||||
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There are no transcripts associated with this gene. |