NM_001015877.1:c.834+53_834+58delAATTTA is an intronic deletion in PHF6 located 53 bases into intron 8, beyond the conserved splice consensus region.1 SpliceAI predicts no significant splice impact (max delta score 0.01), consistent with a benign interpretation (BP4).2 This variant is present in gnomAD v2.1 at low frequency (0.0101%, 18/178,302 alleles) and in gnomAD v4.1 (0.0021%, 25/1,205,804 alleles), below the 0.1% PM2 threshold.3 ClinVar classifies this variant as Benign (Ambry Genetics, criteria provided) and Likely benign (PreventionGenetics), supporting a benign interpretation (BP6).4 The intronic deletion at +53 position is well outside the conserved splice donor/acceptor consensus, and SpliceAI confirms no predicted splice effect (BP7).5 With three supporting benign criteria (BP4, BP6, BP7) met, exceeding the two supporting benign criteria threshold for Likely Benign under generic ACMG/AMP 2015 combination rules, the variant is classified as Likely Benign.6
PHF6
Final classification
Likely Benign
PHF6 c.834+53_834+58del · p.?
PHF6
NM_001015877.1:c.834+53_834+58delAATTTA is an intronic deletion in PHF6 located 53 bases into intron 8, beyond the conserved splice consensus region.
gene-specific framework lacked a usable explicit final combination framework, so generic ACMG/AMP 2015 final-combination rules were applied as fallback; applied criteria: PM2 supporting, BP4 supporting benign, BP6 supporting benign, BP7 supporting benign; combination = 1 supporting + 3 supporting benign, which maps to Likely Benign.
Classification rationale
PM2
BP4BP6BP7
Likely Benign
PHF6 c.834+53_834+58del
PM2 + BP4 + BP6 + BP7
→
Likely Benign
6
generic_acmg_combination_rules
Gene diagram
· NM_001015877.1 · variants mapped to exon structure
PHF6
NM_001015877.1
Fetching transcript structure from UCSC…
Applied criteria · 4 met · select any tile
Met
Not met
Not assessed
N/A
Strength
very strong
supporting
Pathogenic evidence
PVS
PS
PM
PP
Benign evidence
BA
BS
BP
—
—
—
Rationale
Select a criterion.
Sources
Evidence used
Gaps remaining
Rule
—
Research & evidence
Population frequency · supports benign
gnomAD v4.1
gnomAD v2.1
v4.1
This variant is present in gnomAD v4.1 (AF= 2.07331e-05; MAF= 0.00207%, 25/1205804 alleles, homozygotes = 0) and has highest observed frequency in the Admixed American population (AF= 0.000508692; MAF= 0.05087%, 23/45214 alleles, homozygotes = 0); grpmax FAF= 0.00034725.
v2.1
This variant is present in gnomAD v2.1 (AF= 0.000100952; MAF= 0.01010%, 18/178302 alleles, homozygotes = 0) and has highest observed frequency in the Admixed American population (AF= 0.000682568; MAF= 0.06826%, 18/26371 alleles, homozygotes = 0); grpmax FAF= 0.00044099.
🇨🇦 CA
Absent from gnomAD-Canada v1.0.
Allele frequency by ancestry
three datasets · side by side
gnomAD v4.1
0.0021%
· 25 / 1,205,804
0 hom · FAF 0.035%
0 hom · FAF 0.035%
Admixed American 23 / 45,214 |
0.051% |
African/African American 1 / 57,160 |
0.0017% |
European (non-Finnish) 1 / 893,105 |
0.00011% |
+ 7 not observed (Remaining individuals, European (Finnish), Amish, East Asian, Middle Eastern, South Asian, Ashkenazi Jewish)
gnomAD v2.1
0.01%
· 18 / 178,302
0 hom · FAF 0.044%
0 hom · FAF 0.044%
Admixed American 18 / 26,371 |
0.068% |
+ 7 not observed (African/African American, Ashkenazi Jewish, East Asian, European (Finnish), European (non-Finnish), Remaining individuals, South Asian)
gnomAD Canada 🇨🇦
Absent
· 0 / ?
0 hom
0 hom
Not observed in any ancestry group.
ClinVar
This variant has been reported in ClinVar as Benign (1 clinical laboratory) and as Likely benign (1 clinical laboratory). (ClinVarID = 2396348)
In silico
SpliceAI predicts no significant splice impact for this variant (max delta score = 0.01).
Functional
No data
No calibrated functional assay or RNA evidence was identified for this variant.
COSMIC
Somatic evidence
COSMIC
This variant has not previously been reported in somatic cancers (COSMIC).
Hotspots
This variant does not lie in a statistically significant cancer hotspot.
Sources & reference links
Triaged references · 5 PMIDs not cited in assessment
23169492 ↗
The perspective from EASAC and FEAM on direct-to-consumer genetic testing for health-related purposes.
CLINVAR
23037933 ↗
Including the initial newborn screening bloodspot collection device serial number on birth certificates: basis and recommendations from the Secretary of Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children.
CLINVAR
24022298 ↗
Offering prenatal diagnostic tests: European guidelines for clinical practice [corrected].
CLINVAR
24394680 ↗
Parental permission for pilot newborn screening research: guidelines from the NBSTRN.
CLINVAR
31022120 ↗
ACOG Committee Opinion No. 778 Summary: Newborn Screening and the Role of the Obstetrician-Gynecologist.
CLINVAR