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GCTGAAGTCTCTGTTTCCTTGGCTG[C/T]TAAAATAGGGTTTAAAGTGTTTACC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602037 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
N4BP2 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)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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N4BP2 - NEDD4 binding protein 2 | ||||||
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There are no transcripts associated with this gene. |
RHOH - ras homolog family member H | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278359.1 | Intron | NP_001265288.1 | ||||
NM_001278360.1 | Intron | NP_001265289.1 | ||||
NM_001278361.1 | Intron | NP_001265290.1 | ||||
NM_001278362.1 | Intron | NP_001265291.1 | ||||
NM_001278363.1 | Intron | NP_001265292.1 | ||||
NM_001278364.1 | Intron | NP_001265293.1 | ||||
NM_001278365.1 | Intron | NP_001265294.1 | ||||
NM_001278366.1 | Intron | NP_001265295.1 | ||||
NM_001278367.1 | Intron | NP_001265296.1 | ||||
NM_001278368.1 | Intron | NP_001265297.1 | ||||
NM_001278369.1 | Intron | NP_001265298.1 | ||||
NM_004310.4 | Intron | NP_004301.1 | ||||
XM_011513692.1 | Intron | XP_011511994.1 | ||||
XM_017008188.1 | Intron | XP_016863677.1 | ||||
XM_017008189.1 | Intron | XP_016863678.1 |
Set Membership: |
HapMap |