Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCAGCAGGCCAGGGGGAGCTGTGG[A/G]CAGGGCCGTCAGGGGTGGCGAGAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606917 MIM: 607726 MIM: 608503 | ||||||||||||||||||||
Literature Links: |
GPR62 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 |
GPR62 - G protein-coupled receptor 62 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_080865.3 | 1368 | Intron | NP_543141.3 |
PARP3 - poly(ADP-ribose) polymerase family member 3 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
PCBP4 - poly(rC) binding protein 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001174100.1 | 1368 | Missense Mutation | CCC,TCC | P,S 339 | NP_001167571.1 | |
NM_020418.3 | 1368 | Missense Mutation | CCC,TCC | P,S 296 | NP_065151.2 | |
NM_033008.2 | 1368 | Missense Mutation | CCC,TCC | P,S 339 | NP_127501.1 | |
NM_033010.2 | 1368 | Missense Mutation | CCC,TCC | P,S 339 | NP_127503.1 | |
XM_005265330.2 | 1368 | Missense Mutation | CCC,TCC | P,S 362 | XP_005265387.1 | |
XM_005265331.2 | 1368 | Missense Mutation | CCC,TCC | P,S 339 | XP_005265388.1 | |
XM_005265332.2 | 1368 | Missense Mutation | CCC,TCC | P,S 319 | XP_005265389.1 | |
XM_006713268.2 | 1368 | Missense Mutation | CCC,TCC | P,S 339 | XP_006713331.1 | |
XM_006713269.1 | 1368 | Missense Mutation | CCC,TCC | P,S 339 | XP_006713332.1 | |
XM_006713270.1 | 1368 | Missense Mutation | CCC,TCC | P,S 296 | XP_006713333.1 | |
XM_006713271.2 | 1368 | Intron | XP_006713334.1 | |||
XM_017006916.1 | 1368 | Missense Mutation | CCC,TCC | P,S 362 | XP_016862405.1 | |
XM_017006917.1 | 1368 | Intron | XP_016862406.1 | |||
XM_017006918.1 | 1368 | Intron | XP_016862407.1 | |||
XM_017006919.1 | 1368 | Intron | XP_016862408.1 | |||
XM_017006920.1 | 1368 | Intron | XP_016862409.1 |