Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGACCAATGGCAGCAAACAGCTCCC[A/G]GCTCCCTTGAACAGCCATGCCCACG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609912 MIM: 610560 MIM: 600823 | ||||||||||||||||||||
Literature Links: |
KAT8 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 |
KAT8 - lysine acetyltransferase 8 | ||||||
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There are no transcripts associated with this gene. |
PRSS36 - protease, serine 36 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258290.1 | 2118 | Missense Mutation | CGG,TGG | R,W 785 | NP_001245219.1 | |
NM_001258291.1 | 2118 | Missense Mutation | CGG,TGG | R,W 687 | NP_001245220.1 | |
NM_173502.4 | 2118 | Missense Mutation | CGG,TGG | R,W 790 | NP_775773.2 | |
XM_011545758.2 | 2118 | Missense Mutation | CGG,TGG | R,W 565 | XP_011544060.1 | |
XM_017022968.1 | 2118 | Intron | XP_016878457.1 | |||
XM_017022969.1 | 2118 | Intron | XP_016878458.1 | |||
XM_017022970.1 | 2118 | UTR 3 | XP_016878459.1 | |||
XM_017022971.1 | 2118 | Missense Mutation | CCG,CTG | P,L 613 | XP_016878460.1 |
PRSS8 - protease, serine 8 | ||||||
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There are no transcripts associated with this gene. |