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TTTTCAGGCTTACAAGGCTTTCTTT[A/C]CCTTGACATCTTCTTAGATGATGTC
Species: |
Human | |||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 616423 | |||||||||||||||||||||||||||||
Literature Links: |
DHX30 PubMed Links | |||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian
|
CEPH (CEU) - Not Available | ||||||
EAS - Not Available | African American
|
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 |
DHX30 - DEAH-box helicase 30 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014966.3 | Intron | NP_055781.2 | ||||
NM_138615.2 | Intron | NP_619520.1 | ||||
XM_006713033.1 | Intron | XP_006713096.1 | ||||
XM_011533490.1 | Intron | XP_011531792.1 | ||||
XM_011533491.1 | Intron | XP_011531793.1 | ||||
XM_011533492.2 | Intron | XP_011531794.1 | ||||
XM_011533493.1 | Intron | XP_011531795.1 | ||||
XM_011533494.2 | Intron | XP_011531796.1 | ||||
XM_011533495.1 | Intron | XP_011531797.1 | ||||
XM_011533496.1 | Intron | XP_011531798.1 | ||||
XM_011533497.2 | Intron | XP_011531799.1 | ||||
XM_011533498.1 | Intron | XP_011531800.1 | ||||
XM_017005914.1 | Intron | XP_016861403.1 | ||||
XM_017005915.1 | Intron | XP_016861404.1 | ||||
XM_017005916.1 | Intron | XP_016861405.1 | ||||
XM_017005917.1 | Intron | XP_016861406.1 |
Set Membership: |
Validated |