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GCAGGAGGCTCTACTCCTGCAAATG[A/G]GTACAGTCTCAGGACAACTTAGCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C20orf141 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
C20orf141 - chromosome 20 open reading frame 141 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256538.1 | 538 | Missense Mutation | AGT,GGT | S,G 122 | NP_001243467.1 | |
NM_080739.2 | 538 | Missense Mutation | AGT,GGT | S,G 122 | NP_542777.1 |
TMEM239 - transmembrane protein 239 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167670.2 | 538 | Intron | NP_001161142.1 | |||
NM_001318207.1 | 538 | Intron | NP_001305136.1 | |||
XM_011529128.2 | 538 | Intron | XP_011527430.1 | |||
XM_011529129.2 | 538 | Intron | XP_011527431.1 |