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TAAATTATGCTTCCTCAGATGAACC[G/T]CACAGCCCTGCATTTTGCAGTGGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ANKDD1B 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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ANKDD1B - ankyrin repeat and death domain containing 1B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001276713.1 | 651 | Missense Mutation | CGC,CTC | R,L 102 | NP_001263642.1 | |
XM_011543618.2 | 651 | Missense Mutation | CGC,CTC | R,L 102 | XP_011541920.1 | |
XM_011543623.2 | 651 | Intron | XP_011541925.1 | |||
XM_017009814.1 | 651 | Missense Mutation | CGC,CTC | R,L 102 | XP_016865303.1 | |
XM_017009815.1 | 651 | Missense Mutation | CGC,CTC | R,L 102 | XP_016865304.1 | |
XM_017009816.1 | 651 | Missense Mutation | CGC,CTC | R,L 102 | XP_016865305.1 | |
XM_017009817.1 | 651 | Missense Mutation | CGC,CTC | R,L 102 | XP_016865306.1 |