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TGACGGAAAACCATATTCAAGAAAT[C/G]AATGCTCAAACCACAGGCCTCCGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603454 | ||||||||||||||||||||
Literature Links: |
CRADD 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 |
CRADD - CASP2 and RIPK1 domain containing adaptor with death domain | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320099.1 | 263 | Silent Mutation | ATC,ATG | I,M 44 | NP_001307028.1 | |
NM_001320100.1 | 263 | Silent Mutation | ATC,ATG | I,M 44 | NP_001307029.1 | |
NM_001320101.1 | 263 | Silent Mutation | ATC,ATG | I,M 44 | NP_001307030.1 | |
NM_003805.4 | 263 | Silent Mutation | ATC,ATG | I,M 44 | NP_003796.1 | |
XM_017020142.1 | 263 | Missense Mutation | ATC,ATG | I,M 44 | XP_016875631.1 | |
XM_017020143.1 | 263 | Missense Mutation | ATC,ATG | I,M 44 | XP_016875632.1 | |
XM_017020144.1 | 263 | Missense Mutation | ATC,ATG | I,M 44 | XP_016875633.1 | |
XM_017020145.1 | 263 | Missense Mutation | ATC,ATG | I,M 44 | XP_016875634.1 |