Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGTGACTGGAAGGATCCAGGGGTG[A/T]CACTGAGGCGCTCTGAGGAACGGCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
14 submissions
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Phenotype: |
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Literature Links: |
DENND4B 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 |
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 | 3977 | Missense Mutation | GAC,GTC | D,V 1140 | NP_055671.2 | |
XM_005245678.4 | 3977 | Missense Mutation | GAC,GTC | D,V 1151 | XP_005245735.1 | |
XM_005245679.2 | 3977 | Missense Mutation | GAC,GTC | D,V 1140 | XP_005245736.1 | |
XM_011510219.1 | 3977 | Missense Mutation | GAC,GTC | D,V 1068 | XP_011508521.1 | |
XM_011510220.2 | 3977 | Missense Mutation | GAC,GTC | D,V 1035 | XP_011508522.1 | |
XM_011510221.2 | 3977 | Missense Mutation | GAC,GTC | D,V 938 | XP_011508523.1 | |
XM_011510222.1 | 3977 | Intron | XP_011508524.1 | |||
XM_017002993.1 | 3977 | Missense Mutation | GAC,GTC | D,V 1060 | XP_016858482.1 |