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AATGCCTGTCCTGACCCCCTTAGGT[G/T]CTGTATCTCACCTTCCTGGGAGCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
18 submissions
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Phenotype: |
MIM: 602746 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC100996583 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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LOC100996583 - uncharacterized LOC100996583 | ||||||
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There are no transcripts associated with this gene. |
LOC115110 - uncharacterized LOC115110 | ||||||
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There are no transcripts associated with this gene. |
TNFRSF14 - TNF receptor superfamily member 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297605.1 | 372 | Silent Mutation | GTG,GTT | V,V 24 | NP_001284534.1 | |
NM_003820.3 | 372 | Silent Mutation | GTG,GTT | V,V 24 | NP_003811.2 | |
XM_006711019.2 | 372 | Silent Mutation | GTG,GTT | V,V 24 | XP_006711082.1 | |
XM_011542383.2 | 372 | Intron | XP_011540685.1 | |||
XM_017002718.1 | 372 | Intron | XP_016858207.1 | |||
XM_017002719.1 | 372 | Intron | XP_016858208.1 | |||
XM_017002720.1 | 372 | UTR 5 | XP_016858209.1 | |||
XM_017002721.1 | 372 | UTR 5 | XP_016858210.1 |