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AGTATTATCATTTTCCAGTCTCTGC[A/G]TCTCATCTTGTCCCATCTGTCCAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615614 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KLHL32 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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KLHL32 - kelch like family member 32 | ||||||
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There are no transcripts associated with this gene. |
MMS22L - MMS22 like, DNA repair protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_198468.2 | 3970 | Missense Mutation | ACG,ATG | T,M 1235 | NP_940870.2 | |
XM_006715430.1 | 3970 | Missense Mutation | ACG,ATG | T,M 1235 | XP_006715493.1 | |
XM_006715432.3 | 3970 | Intron | XP_006715495.1 | |||
XM_011535670.2 | 3970 | Intron | XP_011533972.1 | |||
XM_011535671.2 | 3970 | Intron | XP_011533973.1 | |||
XM_011535672.2 | 3970 | Intron | XP_011533974.1 | |||
XM_011535673.2 | 3970 | Intron | XP_011533975.1 | |||
XM_011535674.2 | 3970 | Intron | XP_011533976.1 | |||
XM_011535675.2 | 3970 | Intron | XP_011533977.1 | |||
XM_011535676.2 | 3970 | Intron | XP_011533978.1 | |||
XM_011535677.2 | 3970 | Intron | XP_011533979.1 | |||
XM_011535678.2 | 3970 | Intron | XP_011533980.1 | |||
XM_011535679.2 | 3970 | Intron | XP_011533981.1 | |||
XM_011535680.2 | 3970 | Intron | XP_011533982.1 | |||
XM_017010656.1 | 3970 | Intron | XP_016866145.1 | |||
XM_017010657.1 | 3970 | Missense Mutation | ACG,ATG | T,M 952 | XP_016866146.1 |