Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATTGGCCTTTAACTGATGAAGTTCA[C/T]CAAATTTCATACTAATATTTTCTAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605445 | ||||||||||||||||||||
Literature Links: |
DLGAP1 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 |
DLGAP1 - DLG associated protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001003809.2 | 1893 | Missense Mutation | GAT,GGT | D,G 587 | NP_001003809.1 | |
NM_001242761.1 | 1893 | Missense Mutation | GAT,GGT | D,G 889 | NP_001229690.1 | |
NM_001242762.1 | 1893 | Missense Mutation | GAT,GGT | D,G 573 | NP_001229691.1 | |
NM_001242763.1 | 1893 | Missense Mutation | GAT,GGT | D,G 611 | NP_001229692.1 | |
NM_001242764.1 | 1893 | Missense Mutation | GAT,GGT | D,G 595 | NP_001229693.1 | |
NM_001242765.1 | 1893 | Missense Mutation | GAT,GGT | D,G 587 | NP_001229694.1 | |
NM_001242766.1 | 1893 | Missense Mutation | GAT,GGT | D,G 597 | NP_001229695.1 | |
NM_001308390.1 | 1893 | Missense Mutation | GAT,GGT | D,G 605 | NP_001295319.1 | |
NM_004746.3 | 1893 | Missense Mutation | GAT,GGT | D,G 889 | NP_004737.2 | |
XM_005258171.2 | 1893 | Missense Mutation | GAT,GGT | D,G 899 | XP_005258228.1 | |
XM_005258172.1 | 1893 | Missense Mutation | GAT,GGT | D,G 899 | XP_005258229.1 | |
XM_005258173.3 | 1893 | Missense Mutation | GAT,GGT | D,G 676 | XP_005258230.2 | |
XM_005258174.4 | 1893 | Missense Mutation | GAT,GGT | D,G 607 | XP_005258231.1 | |
XM_006722367.3 | 1893 | Missense Mutation | GAT,GGT | D,G 643 | XP_006722430.1 | |
XM_011525770.2 | 1893 | Intron | XP_011524072.1 | |||
XM_011525771.2 | 1893 | Intron | XP_011524073.1 | |||
XM_017026080.1 | 1893 | Missense Mutation | GAT,GGT | D,G 633 | XP_016881569.1 | |
XM_017026081.1 | 1893 | Missense Mutation | GAT,GGT | D,G 601 | XP_016881570.1 | |
XM_017026082.1 | 1893 | Missense Mutation | GAT,GGT | D,G 666 | XP_016881571.1 | |
XM_017026083.1 | 1893 | Missense Mutation | GAT,GGT | D,G 597 | XP_016881572.1 | |
XM_017026084.1 | 1893 | Missense Mutation | GAT,GGT | D,G 597 | XP_016881573.1 | |
XM_017026085.1 | 1893 | Missense Mutation | GAT,GGT | D,G 595 | XP_016881574.1 |