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GGTTCTCGTGTCTCCAAATTACCAC[C/T]GTGGCTAGGCTGCTGGAAAAAAGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604597 MIM: 614539 | ||||||||||||||||||||
Literature Links: |
GRIP1 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 |
GRIP1 - glutamate receptor interacting protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001178074.1 | 3507 | Missense Mutation | AGT,GGT | S,G 1049 | NP_001171545.1 | |
NM_021150.3 | 3507 | Missense Mutation | AGT,GGT | S,G 1064 | NP_066973.2 | |
XM_005268754.4 | 3507 | Missense Mutation | AGT,GGT | S,G 1117 | XP_005268811.1 | |
XM_005268757.4 | 3507 | Missense Mutation | AGT,GGT | S,G 1090 | XP_005268814.1 | |
XM_011538093.2 | 3507 | Missense Mutation | AGT,GGT | S,G 1116 | XP_011536395.1 | |
XM_017019098.1 | 3507 | Missense Mutation | AGT,GGT | S,G 1176 | XP_016874587.1 | |
XM_017019099.1 | 3507 | Missense Mutation | AGT,GGT | S,G 1142 | XP_016874588.1 | |
XM_017019100.1 | 3507 | Missense Mutation | AGT,GGT | S,G 1124 | XP_016874589.1 | |
XM_017019101.1 | 3507 | Missense Mutation | AGT,GGT | S,G 1090 | XP_016874590.1 | |
XM_017019102.1 | 3507 | Missense Mutation | AGT,GGT | S,G 1089 | XP_016874591.1 |
HELB - DNA helicase B | ||||||
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There are no transcripts associated with this gene. |