Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TAAGTGTAATAGGCTACAACATCCA[C/T]GGTAAGTACTAAGTGAAATTATTTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 611690 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRRG4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
PRRG4 - proline rich and Gla domain 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024081.5 | 559 | Missense Mutation | CGC,TGC | R,C 150 | NP_076986.1 | |
XM_006718313.3 | 559 | Intron | XP_006718376.3 | |||
XM_006718314.3 | 559 | Missense Mutation | CGC,TGC | R,C 150 | XP_006718377.1 | |
XM_017018275.1 | 559 | Missense Mutation | CGC,TGC | R,C 288 | XP_016873764.1 |