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TCGAACCAGGCGTTCATCCAGCACA[C/T]GGACGACCACCTTCTCCCCAGCCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604520 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TNFSF14 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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TNFSF14 - tumor necrosis factor superfamily member 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003807.4 | 1035 | Missense Mutation | CAT,CGT | H,R 218 | NP_003798.2 | |
NM_172014.3 | 1035 | Missense Mutation | CAT,CGT | H,R 182 | NP_742011.2 | |
XM_017027417.1 | 1035 | Missense Mutation | CAT,CGT | H,R 218 | XP_016882906.1 | |
XM_017027418.1 | 1035 | Intron | XP_016882907.1 |