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AGCGTTGCTATAATGTATTAGTGGG[A/T]TCTCGTGTCTCCAAATTACCACCGT
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | 3530 | Missense Mutation | GAA,GAT | E,D 1056 | NP_001171545.1 | |
NM_021150.3 | 3530 | Missense Mutation | GAA,GAT | E,D 1071 | NP_066973.2 | |
XM_005268754.4 | 3530 | Missense Mutation | GAA,GAT | E,D 1124 | XP_005268811.1 | |
XM_005268757.4 | 3530 | Missense Mutation | GAA,GAT | E,D 1097 | XP_005268814.1 | |
XM_011538093.2 | 3530 | Missense Mutation | GAA,GAT | E,D 1123 | XP_011536395.1 | |
XM_017019098.1 | 3530 | Missense Mutation | GAA,GAT | E,D 1183 | XP_016874587.1 | |
XM_017019099.1 | 3530 | Missense Mutation | GAA,GAT | E,D 1149 | XP_016874588.1 | |
XM_017019100.1 | 3530 | Missense Mutation | GAA,GAT | E,D 1131 | XP_016874589.1 | |
XM_017019101.1 | 3530 | Missense Mutation | GAA,GAT | E,D 1097 | XP_016874590.1 | |
XM_017019102.1 | 3530 | Missense Mutation | GAA,GAT | E,D 1096 | XP_016874591.1 |
HELB - DNA helicase B | ||||||
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There are no transcripts associated with this gene. |