Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GATTGTGCCATTTCCCTGTTTCAGA[C/T]TGAATGATTGCTGTAACTGATATAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601116 | ||||||||||||||||||||
Literature Links: |
GRM8 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 |
GRM8 - glutamate metabotropic receptor 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000845.2 | 3586 | Missense Mutation | ATC,GTC | I,V 908 | NP_000836.2 | |
NM_001127323.1 | 3586 | UTR 3 | NP_001120795.1 | |||
XM_006715938.3 | 3586 | Missense Mutation | ATC,GTC | I,V 908 | XP_006716001.1 | |
XM_011516091.1 | 3586 | Missense Mutation | ATC,GTC | I,V 908 | XP_011514393.1 | |
XM_011516092.2 | 3586 | UTR 3 | XP_011514394.1 | |||
XM_011516094.1 | 3586 | UTR 3 | XP_011514396.1 | |||
XM_011516095.2 | 3586 | UTR 3 | XP_011514397.1 | |||
XM_011516101.2 | 3586 | UTR 3 | XP_011514403.1 | |||
XM_011516102.2 | 3586 | UTR 3 | XP_011514404.1 | |||
XM_011516103.2 | 3586 | UTR 3 | XP_011514405.1 | |||
XM_011516108.2 | 3586 | UTR 3 | XP_011514410.1 | |||
XM_017012074.1 | 3586 | Missense Mutation | ATC,GTC | I,V 908 | XP_016867563.1 | |
XM_017012075.1 | 3586 | Missense Mutation | ATC,GTC | I,V 703 | XP_016867564.1 | |
XM_017012076.1 | 3586 | Missense Mutation | ATC,GTC | I,V 703 | XP_016867565.1 | |
XM_017012077.1 | 3586 | Missense Mutation | ATC,GTC | I,V 703 | XP_016867566.1 | |
XM_017012078.1 | 3586 | Missense Mutation | ATC,GTC | I,V 703 | XP_016867567.1 | |
XM_017012079.1 | 3586 | Missense Mutation | ATC,GTC | I,V 703 | XP_016867568.1 | |
XM_017012080.1 | 3586 | UTR 3 | XP_016867569.1 |