Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCAGCCCTGGCTGAGGGGCCCATCA[C/T]GATGTTGACGCTGCTGGATGACTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
NTPCR PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
NTPCR - nucleoside-triphosphatase, cancer-related | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
PCNX2 - pecanex homolog 2 (Drosophila) | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014801.3 | 5998 | Missense Mutation | ATG,GTG | M,V 2067 | NP_055616.3 | |
XM_006711816.3 | 5998 | Intron | XP_006711879.1 | |||
XM_011544278.2 | 5998 | Missense Mutation | ATG,GTG | M,V 1325 | XP_011542580.2 | |
XM_017002391.1 | 5998 | Missense Mutation | ATG,GTG | M,V 1864 | XP_016857880.1 | |
XM_017002392.1 | 5998 | Missense Mutation | ATG,GTG | M,V 921 | XP_016857881.1 |