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GCCTGGCTGCGGTCAGGGGTCCCGC[A/G]GGGCGGCTCAAGGAGCAGGGAGCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613619 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KLHL22 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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KLHL22 - kelch like family member 22 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032775.3 | 4524 | Missense Mutation | CGC,TGC | R,C 603 | NP_116164.2 | |
XM_017029018.1 | 4524 | Missense Mutation | CGC,TGC | R,C 671 | XP_016884507.1 | |
XM_017029019.1 | 4524 | Missense Mutation | CGC,TGC | R,C 651 | XP_016884508.1 | |
XM_017029020.1 | 4524 | Missense Mutation | CGC,TGC | R,C 635 | XP_016884509.1 | |
XM_017029021.1 | 4524 | Missense Mutation | CGC,TGC | R,C 603 | XP_016884510.1 | |
XM_017029022.1 | 4524 | Missense Mutation | CGC,TGC | R,C 585 | XP_016884511.1 | |
XM_017029023.1 | 4524 | Missense Mutation | CGC,TGC | R,C 569 | XP_016884512.1 | |
XM_017029024.1 | 4524 | Missense Mutation | CGC,TGC | R,C 563 | XP_016884513.1 | |
XM_017029025.1 | 4524 | Missense Mutation | CGC,TGC | R,C 526 | XP_016884514.1 |
SCARF2 - scavenger receptor class F member 2 | ||||||
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There are no transcripts associated with this gene. |