rs3131628
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Variant summary
Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_StrongBA1
The NM_004640.7(DDX39B):c.735+377G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.847 in 283,868 control chromosomes in the GnomAD database, including 102,380 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.
Frequency
Genomes: 𝑓 0.85 ( 54737 hom., cov: 30)
Exomes 𝑓: 0.85 ( 47643 hom. )
Consequence
DDX39B
NM_004640.7 intron
NM_004640.7 intron
Scores
2
Clinical Significance
Not reported in ClinVar
Conservation
PhyloP100: 0.168
Genes affected
DDX39B (HGNC:13917): (DExD-box helicase 39B) This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011]
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ACMG classification
Classification made for transcript
Verdict is Benign. Variant got -12 ACMG points.
BP4
?
Computational evidence support a benign effect (BayesDel_noAF=-0.49).
BA1
?
GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.904 is higher than 0.05.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
DDX39B | NM_004640.7 | c.735+377G>A | intron_variant | ENST00000396172.6 | |||
ATP6V1G2-DDX39B | NR_037853.1 | n.1538+377G>A | intron_variant, non_coding_transcript_variant | ||||
DDX39B | NM_080598.6 | c.735+377G>A | intron_variant | ||||
DDX39B | NR_037852.2 | n.700+377G>A | intron_variant, non_coding_transcript_variant |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
DDX39B | ENST00000396172.6 | c.735+377G>A | intron_variant | 1 | NM_004640.7 | P1 |
Frequencies
GnomAD3 genomes ? AF: 0.847 AC: 128808AN: 152004Hom.: 54680 Cov.: 30
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GnomAD4 exome AF: 0.847 AC: 111595AN: 131746Hom.: 47643 Cov.: 0 AF XY: 0.857 AC XY: 60104AN XY: 70174
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GnomAD4 genome ? AF: 0.847 AC: 128923AN: 152122Hom.: 54737 Cov.: 30 AF XY: 0.852 AC XY: 63342AN XY: 74368
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ClinVar
Not reported inComputational scores
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Name
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BayesDel_noAF
Benign
CADD
Benign
DANN
Benign
Splicing
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Details are displayed if max score is > 0.2
Find out detailed SpliceAI scores and Pangolin per-transcript scores at