Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GACCCCCGTAGTCCACCAAACTGCA[C/G]GGGTGCAGGCGCCCTTTGGTTTGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 604140 | ||||||||||||||||||||
Literature Links: |
DIDO1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
DIDO1 - death inducer-obliterator 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193369.1 | 6291 | Missense Mutation | CTG,GTG | L,V 1987 | NP_001180298.1 | |
NM_001193370.1 | 6291 | Intron | NP_001180299.1 | |||
NM_022105.4 | 6291 | Intron | NP_071388.2 | |||
NM_033081.2 | 6291 | Missense Mutation | CTG,GTG | L,V 1987 | NP_149072.2 | |
NM_080796.3 | 6291 | Intron | NP_542986.1 | |||
NM_080797.3 | 6291 | Intron | NP_542987.2 | |||
XM_011528504.1 | 6291 | Missense Mutation | CTG,GTG | L,V 2023 | XP_011526806.1 | |
XM_011528505.1 | 6291 | Missense Mutation | CTG,GTG | L,V 2023 | XP_011526807.1 | |
XM_011528506.1 | 6291 | Missense Mutation | CTG,GTG | L,V 2023 | XP_011526808.1 | |
XM_011528507.1 | 6291 | Missense Mutation | CTG,GTG | L,V 2023 | XP_011526809.1 | |
XM_011528508.1 | 6291 | Missense Mutation | CTG,GTG | L,V 2023 | XP_011526810.1 | |
XM_011528509.2 | 6291 | Missense Mutation | CTG,GTG | L,V 1987 | XP_011526811.1 |