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CCGCCACAGCCTCAGCCAGACATCG[G/T]TCATGAAGCTGCCCCTGCTCGGTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
13 submissions
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Phenotype: |
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Literature Links: |
NTPCR 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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NTPCR - nucleoside-triphosphatase, cancer-related | ||||||
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There are no transcripts associated with this gene. |
PCNX2 - pecanex homolog 2 (Drosophila) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014801.3 | 6096 | Missense Mutation | GAA,GAC | E,D 2099 | NP_055616.3 | |
XM_006711816.3 | 6096 | Intron | XP_006711879.1 | |||
XM_011544278.2 | 6096 | Missense Mutation | GAA,GAC | E,D 1357 | XP_011542580.2 | |
XM_017002391.1 | 6096 | Missense Mutation | GAA,GAC | E,D 1896 | XP_016857880.1 | |
XM_017002392.1 | 6096 | Missense Mutation | GAA,GAC | E,D 953 | XP_016857881.1 |