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TGAGATAACAGATTGATCGCAGAAG[A/T]CTCCTGGGCCAGCCTGCCAACCTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 600178 MIM: 610979 | ||||||||||||||||||||
Literature Links: |
MAP1A 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 |
MAP1A - microtubule associated protein 1A | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
PPIP5K1 - diphosphoinositol pentakisphosphate kinase 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130858.2 | 4381 | Missense Mutation | ACT,TCT | T,S 1397 | NP_001124330.1 | |
NM_001130859.2 | 4381 | Missense Mutation | ACT,TCT | T,S 1372 | NP_001124331.1 | |
NM_001190214.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1370 | NP_001177143.1 | |
NM_014659.5 | 4381 | Missense Mutation | ACT,TCT | T,S 1372 | NP_055474.3 | |
XM_005254803.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1393 | XP_005254860.1 | |
XM_005254804.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1372 | XP_005254861.1 | |
XM_006720786.2 | 4381 | Missense Mutation | ACT,TCT | T,S 1330 | XP_006720849.1 | |
XM_011522249.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1443 | XP_011520551.1 | |
XM_011522250.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1443 | XP_011520552.1 | |
XM_011522252.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1443 | XP_011520554.1 | |
XM_011522254.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1443 | XP_011520556.1 | |
XM_011522258.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1188 | XP_011520560.1 | |
XM_011522259.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1385 | XP_011520561.1 | |
XM_017022735.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1443 | XP_016878224.1 | |
XM_017022736.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1443 | XP_016878225.1 | |
XM_017022737.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1443 | XP_016878226.1 | |
XM_017022738.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1435 | XP_016878227.1 | |
XM_017022739.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1422 | XP_016878228.1 | |
XM_017022740.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1393 | XP_016878229.1 | |
XM_017022741.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1393 | XP_016878230.1 | |
XM_017022742.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1393 | XP_016878231.1 | |
XM_017022743.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1393 | XP_016878232.1 | |
XM_017022744.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1393 | XP_016878233.1 | |
XM_017022745.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1385 | XP_016878234.1 | |
XM_017022746.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1385 | XP_016878235.1 | |
XM_017022747.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1380 | XP_016878236.1 | |
XM_017022748.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1372 | XP_016878237.1 | |
XM_017022749.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1372 | XP_016878238.1 | |
XM_017022750.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1372 | XP_016878239.1 | |
XM_017022751.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1372 | XP_016878240.1 | |
XM_017022752.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1364 | XP_016878241.1 | |
XM_017022753.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1364 | XP_016878242.1 | |
XM_017022754.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1330 | XP_016878243.1 | |
XM_017022755.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1330 | XP_016878244.1 | |
XM_017022756.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1330 | XP_016878245.1 | |
XM_017022757.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1330 | XP_016878246.1 | |
XM_017022758.1 | 4381 | Missense Mutation | ACT,TCT | T,S 1117 | XP_016878247.1 | |
XM_017022759.1 | 4381 | Intron | XP_016878248.1 | |||
XM_017022760.1 | 4381 | Missense Mutation | ACT,TCT | T,S 729 | XP_016878249.1 |