chr6-31166398-C-T
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Variant summary
Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_StrongBA1
The ENST00000471529.6(POU5F1):c.-534G>A variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.52 in 1,382,474 control chromosomes in the GnomAD database, including 188,093 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 0.54 ( 22913 hom., cov: 33)
Exomes 𝑓: 0.52 ( 165180 hom. )
Consequence
POU5F1
ENST00000471529.6 5_prime_UTR
ENST00000471529.6 5_prime_UTR
Scores
2
Clinical Significance
Not reported in ClinVar
Conservation
PhyloP100: -1.25
Genes affected
POU5F1 (HGNC:9221): (POU class 5 homeobox 1) This gene encodes a transcription factor containing a POU homeodomain that plays a key role in embryonic development and stem cell pluripotency. Aberrant expression of this gene in adult tissues is associated with tumorigenesis. This gene can participate in a translocation with the Ewing's sarcoma gene on chromosome 21, which also leads to tumor formation. Alternative splicing, as well as usage of alternative AUG and non-AUG translation initiation codons, results in multiple isoforms. One of the AUG start codons is polymorphic in human populations. Related pseudogenes have been identified on chromosomes 1, 3, 8, 10, and 12. [provided by RefSeq, Oct 2013]
TCF19 (HGNC:11629): (transcription factor 19) This gene encodes a protein that contains a PHD-type zinc finger domain and likely functions as a transcription factor. The encoded protein plays a role proliferation and apoptosis of pancreatic beta cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
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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=-0.91).
BA1
GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.625 is higher than 0.05.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
POU5F1 | NM_002701.6 | c.406-351G>A | intron_variant | ENST00000259915.13 | |||
POU5F1 | NM_001285986.2 | c.-759G>A | 5_prime_UTR_variant | 1/3 | |||
POU5F1 | NM_203289.6 | c.-456G>A | 5_prime_UTR_variant | 1/4 | |||
POU5F1 | NM_001173531.3 | c.-106+136G>A | intron_variant |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
POU5F1 | ENST00000259915.13 | c.406-351G>A | intron_variant | 1 | NM_002701.6 | P1 |
Frequencies
GnomAD3 genomes AF: 0.545 AC: 82757AN: 151882Hom.: 22909 Cov.: 33
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GnomAD3 exomes AF: 0.520 AC: 65344AN: 125642Hom.: 17462 AF XY: 0.520 AC XY: 35801AN XY: 68846
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GnomAD4 exome AF: 0.516 AC: 635417AN: 1230474Hom.: 165180 Cov.: 42 AF XY: 0.516 AC XY: 310249AN XY: 601390
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GnomAD4 genome AF: 0.545 AC: 82791AN: 152000Hom.: 22913 Cov.: 33 AF XY: 0.542 AC XY: 40245AN XY: 74288
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ClinVar
Not reported inComputational scores
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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