Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTCATCTCCACTCTGCAGTACCTCA[A/G]TCTCATCAACTACTACAAGGTAGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601409 MIM: 610330 | ||||||||||||||||||||
Literature Links: |
KAT5 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 |
KAT5 - lysine acetyltransferase 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206833.1 | 1523 | Missense Mutation | AAT,AGT | N,S 444 | NP_001193762.1 | |
NM_006388.3 | 1523 | Missense Mutation | AAT,AGT | N,S 463 | NP_006379.2 | |
NM_182709.2 | 1523 | Missense Mutation | AAT,AGT | N,S 411 | NP_874368.1 | |
NM_182710.2 | 1523 | Missense Mutation | AAT,AGT | N,S 496 | NP_874369.1 | |
XM_006718421.2 | 1523 | Missense Mutation | AAT,AGT | N,S 472 | XP_006718484.1 |
RNASEH2C - ribonuclease H2 subunit C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032193.3 | 1523 | UTR 3 | NP_115569.2 |