Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTTGGGGTGTCTTCCTCACTGATA[C/G]TGCAAGCTGTGACTTGGTGGTCAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CWH43 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 |
CWH43 - cell wall biogenesis 43 C-terminal homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286791.1 | 530 | Missense Mutation | CTG,GTG | L,V 79 | NP_001273720.1 | |
NM_025087.2 | 530 | Missense Mutation | CTG,GTG | L,V 106 | NP_079363.2 | |
XM_011513755.1 | 530 | Missense Mutation | CTG,GTG | L,V 106 | XP_011512057.1 | |
XM_011513756.2 | 530 | Missense Mutation | CTG,GTG | L,V 79 | XP_011512058.1 | |
XM_011513757.2 | 530 | Missense Mutation | CTG,GTG | L,V 79 | XP_011512059.1 | |
XM_011513758.1 | 530 | Missense Mutation | CTG,GTG | L,V 106 | XP_011512060.1 | |
XM_011513759.1 | 530 | UTR 5 | XP_011512061.1 |