Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGATGAATTAGTCGGTTGGCACTTA[C/T]GAACACATTTATTGCCCTGTTTAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609118 | ||||||||||||||||||||
Literature Links: |
PDCD10 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 |
PDCD10 - programmed cell death 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_007217.3 | 1703 | Missense Mutation | NP_009148.2 | |||
NM_145859.1 | 1703 | Intron | NP_665858.1 | |||
NM_145860.1 | 1703 | Intron | NP_665859.1 | |||
XM_005247086.4 | 1703 | Missense Mutation | XP_005247143.1 | |||
XM_005247087.4 | 1703 | Missense Mutation | XP_005247144.1 | |||
XM_005247088.3 | 1703 | Missense Mutation | XP_005247145.1 | |||
XM_006713485.3 | 1703 | Missense Mutation | XP_006713548.1 | |||
XM_011512368.2 | 1703 | Missense Mutation | XP_011510670.1 | |||
XM_011512369.2 | 1703 | Missense Mutation | XP_011510671.1 | |||
XM_017005644.1 | 1703 | Missense Mutation | XP_016861133.1 | |||
XM_017005645.1 | 1703 | Missense Mutation | XP_016861134.1 |