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CGAAGGCCCATCACAGGAGGCCAGC[A/G]CCAGGCCTGGTAGAATACTGGGCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 614998 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DENND4B 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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DENND4B - DENN domain containing 4B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014856.2 | 4520 | Missense Mutation | GCG,GTG | A,V 1321 | NP_055671.2 | |
XM_005245678.4 | 4520 | Missense Mutation | GCG,GTG | A,V 1332 | XP_005245735.1 | |
XM_005245679.2 | 4520 | Missense Mutation | GCG,GTG | A,V 1321 | XP_005245736.1 | |
XM_011510219.1 | 4520 | Missense Mutation | GCG,GTG | A,V 1249 | XP_011508521.1 | |
XM_011510220.2 | 4520 | Missense Mutation | GCG,GTG | A,V 1216 | XP_011508522.1 | |
XM_011510221.2 | 4520 | Missense Mutation | GCG,GTG | A,V 1119 | XP_011508523.1 | |
XM_011510222.1 | 4520 | Intron | XP_011508524.1 | |||
XM_017002993.1 | 4520 | Missense Mutation | GCG,GTG | A,V 1241 | XP_016858482.1 |
GATAD2B - GATA zinc finger domain containing 2B | ||||||
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There are no transcripts associated with this gene. |