Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGCTTCACCATTGTCTTCCATGGC[C/T]GCCGCTCCAACCTGGACCTGATGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 605939 | ||||||||||||||||||||
Literature Links: |
PLCD4 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 |
PLCD4 - phospholipase C delta 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032726.3 | 631 | Missense Mutation | CGC,TGC | R,C 98 | NP_116115.1 | |
XM_005246913.2 | 631 | Missense Mutation | CGC,TGC | R,C 98 | XP_005246970.1 | |
XM_011512012.1 | 631 | Missense Mutation | CGC,TGC | R,C 98 | XP_011510314.1 | |
XM_017005114.1 | 631 | Missense Mutation | CGC,TGC | R,C 98 | XP_016860603.1 | |
XM_017005115.1 | 631 | Missense Mutation | CGC,TGC | R,C 98 | XP_016860604.1 | |
XM_017005116.1 | 631 | Missense Mutation | CGC,TGC | R,C 98 | XP_016860605.1 | |
XM_017005117.1 | 631 | Missense Mutation | CGC,TGC | R,C 98 | XP_016860606.1 | |
XM_017005118.1 | 631 | UTR 5 | XP_016860607.1 | |||
XM_017005119.1 | 631 | Intron | XP_016860608.1 | |||
XM_017005120.1 | 631 | Intron | XP_016860609.1 |