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GACCCATTTGCTAAGTGATAGTAAA[A/C]ATTCTTCAGTGTTTCAGGATTGACT
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
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
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 | Intron | NP_001003809.1 | ||||
NM_001242761.1 | Intron | NP_001229690.1 | ||||
NM_001242762.1 | Intron | NP_001229691.1 | ||||
NM_001242763.1 | Intron | NP_001229692.1 | ||||
NM_001242764.1 | Intron | NP_001229693.1 | ||||
NM_001242765.1 | Intron | NP_001229694.1 | ||||
NM_001242766.1 | Intron | NP_001229695.1 | ||||
NM_001308390.1 | Intron | NP_001295319.1 | ||||
NM_004746.3 | Intron | NP_004737.2 | ||||
XM_005258171.2 | Intron | XP_005258228.1 | ||||
XM_005258172.1 | Intron | XP_005258229.1 | ||||
XM_005258173.3 | Intron | XP_005258230.2 | ||||
XM_005258174.4 | Intron | XP_005258231.1 | ||||
XM_006722367.3 | Intron | XP_006722430.1 | ||||
XM_011525770.2 | Intron | XP_011524072.1 | ||||
XM_011525771.2 | Intron | XP_011524073.1 | ||||
XM_017026080.1 | Intron | XP_016881569.1 | ||||
XM_017026081.1 | Intron | XP_016881570.1 | ||||
XM_017026082.1 | Intron | XP_016881571.1 | ||||
XM_017026083.1 | Intron | XP_016881572.1 | ||||
XM_017026084.1 | Intron | XP_016881573.1 | ||||
XM_017026085.1 | Intron | XP_016881574.1 |