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GGAGTTTGTTCCTCACAAGGCCTGA[C/T]GGGTAGTCTTCCCCACTTCCGTGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 193040 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
USP37 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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USP37 - ubiquitin specific peptidase 37 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020935.2 | 3304 | Missense Mutation | CAT,CGT | H,R 976 | NP_065986.2 | |
XM_005246720.2 | 3304 | Missense Mutation | CAT,CGT | H,R 976 | XP_005246777.1 | |
XM_005246721.3 | 3304 | Missense Mutation | CAT,CGT | H,R 976 | XP_005246778.1 | |
XM_005246722.3 | 3304 | Missense Mutation | CAT,CGT | H,R 976 | XP_005246779.1 | |
XM_005246724.1 | 3304 | Missense Mutation | CAT,CGT | H,R 954 | XP_005246781.1 | |
XM_011511538.2 | 3304 | Missense Mutation | CAT,CGT | H,R 976 | XP_011509840.1 | |
XM_011511541.2 | 3304 | Intron | XP_011509843.1 | |||
XM_017004577.1 | 3304 | Missense Mutation | CAT,CGT | H,R 728 | XP_016860066.1 |
VIL1 - villin 1 | ||||||
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There are no transcripts associated with this gene. |