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TGCGGGGTATGGGGACTGTTGAGGA[C/T]AACCAGGACTGGGGGCCCTGCCTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 153340 MIM: 610038 | ||||||||||||||||||||
Literature Links: |
CD5 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 |
CD5 - CD5 molecule | ||||||
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There are no transcripts associated with this gene. |
VPS37C - VPS37C, ESCRT-I subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017966.4 | 988 | Missense Mutation | TAT,TGT | Y,C 296 | NP_060436.4 | |
XM_005274077.3 | 988 | Missense Mutation | TAT,TGT | Y,C 296 | XP_005274134.1 | |
XM_017017955.1 | 988 | Missense Mutation | TAT,TGT | Y,C 183 | XP_016873444.1 |