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Search Thermo Fisher Scientific
GGTAGCTCAAGGGAACGGTAGTCAG[C/T]GCTTGTTAAGTCTTGGCTGTCCTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 615788 | ||||||||||||||||||||
Literature Links: |
N4BP2L2 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 |
N4BP2L2 - NEDD4 binding protein 2 like 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278432.1 | 3487 | Missense Mutation | ACT,GCT | T,A 673 | NP_001265361.1 | |
NM_001320836.1 | 3487 | Missense Mutation | ACT,GCT | T,A 1117 | NP_001307765.1 | |
NM_014887.2 | 3487 | Intron | NP_055702.1 | |||
NM_033111.4 | 3487 | Missense Mutation | ACT,GCT | T,A 688 | NP_149102.3 | |
XM_011534869.2 | 3487 | Missense Mutation | ACT,GCT | T,A 673 | XP_011533171.1 | |
XM_011534870.2 | 3487 | Missense Mutation | ACT,GCT | T,A 601 | XP_011533172.1 | |
XM_011534871.2 | 3487 | Missense Mutation | ACT,GCT | T,A 601 | XP_011533173.1 | |
XM_011534872.2 | 3487 | Missense Mutation | ACT,GCT | T,A 571 | XP_011533174.1 | |
XM_011534874.2 | 3487 | Intron | XP_011533176.1 | |||
XM_017020324.1 | 3487 | Missense Mutation | ACT,GCT | T,A 1117 | XP_016875813.1 | |
XM_017020325.1 | 3487 | Missense Mutation | ACT,GCT | T,A 1117 | XP_016875814.1 | |
XM_017020326.1 | 3487 | Missense Mutation | ACT,GCT | T,A 1117 | XP_016875815.1 | |
XM_017020327.1 | 3487 | Missense Mutation | ACT,GCT | T,A 1117 | XP_016875816.1 | |
XM_017020328.1 | 3487 | Missense Mutation | ACT,GCT | T,A 1117 | XP_016875817.1 | |
XM_017020329.1 | 3487 | Missense Mutation | ACT,GCT | T,A 1117 | XP_016875818.1 | |
XM_017020330.1 | 3487 | Missense Mutation | ACT,GCT | T,A 1117 | XP_016875819.1 | |
XM_017020331.1 | 3487 | Missense Mutation | ACT,GCT | T,A 704 | XP_016875820.1 | |
XM_017020332.1 | 3487 | Missense Mutation | ACT,GCT | T,A 704 | XP_016875821.1 | |
XM_017020333.1 | 3487 | Missense Mutation | ACT,GCT | T,A 704 | XP_016875822.1 | |
XM_017020334.1 | 3487 | Missense Mutation | ACT,GCT | T,A 704 | XP_016875823.1 | |
XM_017020335.1 | 3487 | Missense Mutation | ACT,GCT | T,A 673 | XP_016875824.1 | |
XM_017020336.1 | 3487 | Missense Mutation | ACT,GCT | T,A 601 | XP_016875825.1 | |
XM_017020337.1 | 3487 | Missense Mutation | ACT,GCT | T,A 601 | XP_016875826.1 | |
XM_017020338.1 | 3487 | Missense Mutation | ACT,GCT | T,A 601 | XP_016875827.1 | |
XM_017020339.1 | 3487 | Missense Mutation | ACT,GCT | T,A 571 | XP_016875828.1 | |
XM_017020340.1 | 3487 | Missense Mutation | ACT,GCT | T,A 571 | XP_016875829.1 | |
XM_017020341.1 | 3487 | Missense Mutation | ACT,GCT | T,A 571 | XP_016875830.1 | |
XM_017020342.1 | 3487 | Intron | XP_016875831.1 | |||
XM_017020343.1 | 3487 | Missense Mutation | ACT,GCT | T,A 519 | XP_016875832.1 | |
XM_017020344.1 | 3487 | Missense Mutation | ACT,GCT | T,A 519 | XP_016875833.1 | |
XM_017020345.1 | 3487 | Missense Mutation | ACT,GCT | T,A 519 | XP_016875834.1 | |
XM_017020346.1 | 3487 | Missense Mutation | ACT,GCT | T,A 519 | XP_016875835.1 | |
XM_017020347.1 | 3487 | Intron | XP_016875836.1 | |||
XM_017020348.1 | 3487 | Intron | XP_016875837.1 | |||
XM_017020349.1 | 3487 | Intron | XP_016875838.1 |