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GCGTCTCAGCTCGATGATCTCTGCC[C/T]GGCAGGACTGCAACTGCTCTGAGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602760 MIM: 602764 MIM: 604540 | ||||||||||||||||||||
Literature Links: |
KRT32 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
KRT32 - keratin 32 | ||||||
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There are no transcripts associated with this gene. |
KRT35 - keratin 35 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002280.4 | 2575 | Missense Mutation | NP_002271.3 | |||
XM_011524794.1 | 2575 | Missense Mutation | XP_011523096.1 |
KRT36 - keratin 36 | ||||||
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There are no transcripts associated with this gene. |