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GAAAAGCCATATTTCAGTTCTTTTG[A/G]TTCTGGAGCTTCAACTAACAGGAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611119 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KLHL7 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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KLHL7 - kelch like family member 7 | ||||||
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There are no transcripts associated with this gene. |
NUPL2 - nucleoporin like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_007342.2 | 1053 | Missense Mutation | GAT,GGT | D,G 84 | NP_031368.1 | |
XM_005249592.1 | 1053 | Missense Mutation | GAT,GGT | D,G 84 | XP_005249649.1 | |
XM_005249593.3 | 1053 | UTR 5 | XP_005249650.1 | |||
XM_011515104.2 | 1053 | Intron | XP_011513406.1 | |||
XM_017011714.1 | 1053 | UTR 5 | XP_016867203.1 | |||
XM_017011715.1 | 1053 | UTR 5 | XP_016867204.1 | |||
XM_017011716.1 | 1053 | UTR 5 | XP_016867205.1 | |||
XM_017011717.1 | 1053 | Intron | XP_016867206.1 | |||
XM_017011718.1 | 1053 | Intron | XP_016867207.1 |