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TGGGTGGCTATCCAGAGTGTGTCTG[C/T]GTGGCCGGAGAAGAGAGGCGAAATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 169800 | ||||||||||||||||||||
Literature Links: |
CNDP2 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 |
CNDP2 - CNDP dipeptidase 2 (metallopeptidase M20 family) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001168499.1 | 190 | Missense Mutation | GCG,GTG | A,V 33 | NP_001161971.1 | |
NM_018235.2 | 190 | Missense Mutation | GCG,GTG | A,V 33 | NP_060705.2 | |
XM_005266728.2 | 190 | Missense Mutation | GCG,GTG | A,V 33 | XP_005266785.1 | |
XM_006722503.2 | 190 | Missense Mutation | GCG,GTG | A,V 33 | XP_006722566.1 | |
XM_011526071.2 | 190 | Missense Mutation | GCG,GTG | A,V 33 | XP_011524373.1 | |
XM_011526072.2 | 190 | Missense Mutation | GCG,GTG | A,V 33 | XP_011524374.1 | |
XM_011526073.2 | 190 | UTR 5 | XP_011524375.1 |