Product Details
- SNP ID
-
rs199749018
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:146029963 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTGCCTGACGGCCAGTCCCTCCCCC[C/T]AGGCAGGACTAAGAAGCCCATTGCG
- Phenotype
-
MIM: 604473
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
GRM1
PubMed Links
Gene Details
- Gene
- GRM1
- Gene Name
- glutamate metabotropic receptor 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001278064.1 |
925 |
Missense Mutation |
CCA,CTA |
P149L |
NP_001264993.1 |
NM_001278065.1 |
925 |
Missense Mutation |
CCA,CTA |
P149L |
NP_001264994.1 |
NM_001278066.1 |
925 |
Missense Mutation |
CCA,CTA |
P149L |
NP_001264995.1 |
NM_001278067.1 |
925 |
Missense Mutation |
CCA,CTA |
P149L |
NP_001264996.1 |
XM_011535782.1 |
925 |
Missense Mutation |
CCA,CTA |
P149L |
XP_011534084.1 |
XM_017010783.1 |
925 |
Missense Mutation |
CCA,CTA |
P149L |
XP_016866272.1 |
XM_017010784.1 |
925 |
Missense Mutation |
CCA,CTA |
P149L |
XP_016866273.1 |
XM_017010785.1 |
925 |
Missense Mutation |
CCA,CTA |
P149L |
XP_016866274.1 |
XM_017010786.1 |
925 |
Missense Mutation |
CCA,CTA |
P149L |
XP_016866275.1 |
XM_017010787.1 |
925 |
Missense Mutation |
CCA,CTA |
P149L |
XP_016866276.1 |
XM_017010788.1 |
925 |
Intron |
|
|
XP_016866277.1 |
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