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Search Thermo Fisher Scientific
GAAATGCCTTTAACCGGCGTGGGGC[C/T]GGGCAGCTGCAGGAGGCAGATCATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605322 | ||||||||||||||||||||
Literature Links: |
LOC105376777 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 |
LOC105376777 - uncharacterized LOC105376777 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_011523512.2 | 289 | Intron | XP_011521814.1 |
WFDC1 - WAP four-disulfide core domain 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282466.1 | 289 | Missense Mutation | CCG,CTG | P,L 8 | NP_001269395.1 | |
NM_001282467.1 | 289 | Missense Mutation | CCG,CTG | P,L 8 | NP_001269396.1 | |
NM_021197.3 | 289 | Missense Mutation | CCG,CTG | P,L 8 | NP_067020.2 | |
XM_005256079.3 | 289 | Missense Mutation | CCG,CTG | P,L 8 | XP_005256136.1 |