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ATTGAACTCTCCATGCAGTTCTGCT[C/G]AAACATCTGCTCATCAATAAACTCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
|
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Phenotype: |
MIM: 606168 MIM: 605411 | ||||||||||||||||||||
Literature Links: |
DDX20 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 |
DDX20 - DEAD-box helicase 20 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
KCND3 - potassium voltage-gated channel subfamily D member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004980.4 | 2019 | Missense Mutation | CAG,GAG | Q,E 517 | NP_004971.2 | |
NM_172198.2 | 2019 | Missense Mutation | CAG,GAG | Q,E 498 | NP_751948.1 | |
XM_005270851.4 | 2019 | Missense Mutation | CAG,GAG | Q,E 517 | XP_005270908.1 | |
XM_006710629.3 | 2019 | Missense Mutation | CAG,GAG | Q,E 517 | XP_006710692.1 | |
XM_006710630.3 | 2019 | Missense Mutation | CAG,GAG | Q,E 498 | XP_006710693.1 | |
XM_006710631.3 | 2019 | Intron | XP_006710694.1 | |||
XM_006710632.3 | 2019 | Intron | XP_006710695.1 | |||
XM_011541425.2 | 2019 | Intron | XP_011539727.1 | |||
XM_011541426.2 | 2019 | Intron | XP_011539728.1 | |||
XM_011541427.2 | 2019 | Intron | XP_011539729.1 | |||
XM_011541428.2 | 2019 | Intron | XP_011539730.1 | |||
XM_017001244.1 | 2019 | Missense Mutation | CAG,GAG | Q,E 517 | XP_016856733.1 | |
XM_017001245.1 | 2019 | Intron | XP_016856734.1 |