Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAATGTCCAAGCACGTGATGATGGG[A/G]GCCTTATTCCTCTTCATAATGCATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607128 | ||||||||||||||||||||
Literature Links: |
TNKS2 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 |
TNKS2 - tankyrase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_025235.3 | 599 | Missense Mutation | AGC,GGC | S,G 91 | NP_079511.1 | |
XM_005270185.4 | 599 | Missense Mutation | AGC,GGC | S,G 112 | XP_005270242.2 | |
XM_011540213.1 | 599 | Missense Mutation | AGC,GGC | S,G 112 | XP_011538515.1 | |
XM_011540215.2 | 599 | Intron | XP_011538517.1 | |||
XM_017016696.1 | 599 | Missense Mutation | AGC,GGC | S,G 91 | XP_016872185.1 | |
XM_017016697.1 | 599 | UTR 5 | XP_016872186.1 | |||
XM_017016698.1 | 599 | UTR 5 | XP_016872187.1 | |||
XM_017016699.1 | 599 | UTR 5 | XP_016872188.1 | |||
XM_017016700.1 | 599 | UTR 5 | XP_016872189.1 | |||
XM_017016701.1 | 599 | Missense Mutation | AGC,GGC | S,G 112 | XP_016872190.1 |