Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTTTTTCTTTCAGGATTGGAGACA[C/T]AAAATCAGAAATTAAGATTCTAAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605238 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HNMT 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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HNMT - histamine N-methyltransferase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001024074.2 | 236 | Intron | NP_001019245.1 | |||
NM_001024075.1 | 236 | Missense Mutation | ACA,ATA | T,I 50 | NP_001019246.1 | |
NM_006895.2 | 236 | Missense Mutation | ACA,ATA | T,I 50 | NP_008826.1 | |
XM_011511064.2 | 236 | Intron | XP_011509366.1 | |||
XM_017003948.1 | 236 | Missense Mutation | ACA,ATA | T,I 16 | XP_016859437.1 | |
XM_017003949.1 | 236 | Missense Mutation | ACA,ATA | T,I 50 | XP_016859438.1 |