Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGAGGCCTGGAGCCGTCGCCGGCCG[A/C]GGTGGCGGCGCTGCCGCCTGAAGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611379 | ||||||||||||||||||||
Literature Links: |
DIP2B 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 |
DIP2B - disco interacting protein 2 homolog B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173602.2 | 191 | Missense Mutation | GAG,GCG | E,A 12 | NP_775873.2 | |
XM_005269044.1 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_005269101.1 | |
XM_006719520.3 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_006719583.1 | |
XM_006719521.3 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_006719584.1 | |
XM_011538594.2 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_011536896.1 | |
XM_011538595.2 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_011536897.1 | |
XM_011538596.2 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_011536898.1 | |
XM_017019699.1 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_016875188.1 | |
XM_017019700.1 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_016875189.1 | |
XM_017019701.1 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_016875190.1 | |
XM_017019702.1 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_016875191.1 | |
XM_017019703.1 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_016875192.1 | |
XM_017019704.1 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_016875193.1 | |
XM_017019705.1 | 191 | Missense Mutation | GAG,GCG | E,A 12 | XP_016875194.1 |