Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACCTTTGCCAGCTTTGATTCTTTCT[C/T]GCAACTGTTAAGAAACAAATGCATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610564 | ||||||||||||||||||||
Literature Links: |
PDSS2 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 |
PDSS2 - prenyl (decaprenyl) diphosphate synthase, subunit 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020381.3 | 1050 | Missense Mutation | CAA,CGA | Q,R 349 | NP_065114.3 | |
XM_011535956.2 | 1050 | Missense Mutation | CAA,CGA | Q,R 415 | XP_011534258.1 | |
XM_011535957.2 | 1050 | Missense Mutation | CAA,CGA | Q,R 371 | XP_011534259.1 | |
XM_011535958.2 | 1050 | Missense Mutation | CAA,CGA | Q,R 370 | XP_011534260.1 | |
XM_011535959.2 | 1050 | Missense Mutation | CAA,CGA | Q,R 305 | XP_011534261.1 | |
XM_011535960.2 | 1050 | Missense Mutation | CAA,CGA | Q,R 279 | XP_011534262.1 | |
XM_011535961.2 | 1050 | Missense Mutation | CAA,CGA | Q,R 247 | XP_011534263.1 | |
XM_011535962.2 | 1050 | Missense Mutation | CAA,CGA | Q,R 213 | XP_011534264.1 | |
XM_011535963.2 | 1050 | Intron | XP_011534265.1 | |||
XM_017011082.1 | 1050 | Intron | XP_016866571.1 |