Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATGGACTCGGCCCTCAGCGATCCG[C/T]ATAACGGCAGTGCCGAGGCAGGCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607106 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HM13 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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HM13 - histocompatibility minor 13 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030789.3 | 167 | Missense Mutation | CAT,TAT | H,Y 9 | NP_110416.1 | |
NM_178580.2 | 167 | Missense Mutation | CAT,TAT | H,Y 9 | NP_848695.1 | |
NM_178581.2 | 167 | Missense Mutation | CAT,TAT | H,Y 9 | NP_848696.1 | |
NM_178582.2 | 167 | Missense Mutation | CAT,TAT | H,Y 9 | NP_848697.1 |