Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACCAGCCGCTCTGCGGGCAGCTCCT[C/T]TACAGAGCCAGCTGAGGCCACGATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 613247 | ||||||||||||||||||||
Literature Links: |
HDGFRP2 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 |
HDGFRP2 - hepatoma-derived growth factor-related protein 2 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
PLIN4 - perilipin 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080400.1 | 5886 | Missense Mutation | AAG,GAG | K,E 1309 | NP_001073869.1 | |
XM_006722866.2 | 5886 | Missense Mutation | AAG,GAG | K,E 1324 | XP_006722929.1 | |
XM_006722868.3 | 5886 | Missense Mutation | AAG,GAG | K,E 1323 | XP_006722931.1 | |
XM_011528233.2 | 5886 | Missense Mutation | AAG,GAG | K,E 1384 | XP_011526535.1 | |
XM_017027192.1 | 5886 | Missense Mutation | AAG,GAG | K,E 1385 | XP_016882681.1 | |
XM_017027193.1 | 5886 | Missense Mutation | AAG,GAG | K,E 1385 | XP_016882682.1 | |
XM_017027194.1 | 5886 | Missense Mutation | AAG,GAG | K,E 1385 | XP_016882683.1 |