16-30703955-A-C

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_006662.3(SRCAP):c.55-109A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00595 in 1,322,554 control chromosomes in the GnomAD database, including 354 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency:
  • Genomes: 𝑓 0.029 (190 hom., cov: 32)
  • Exomes 𝑓: 0.0029 (164 hom.)
• Consequence: SRCAP NM_006662.3 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.813

Genes affected

SRCAP (HGNC:16974): (Snf2 related CREBBP activator protein) This gene encodes the core catalytic component of the multiprotein chromatin-remodeling SRCAP complex. The encoded protein is an ATPase that is necessary for the incorporation of the histone variant H2A.Z into nucleosomes. It can function as a transcriptional activator in Notch-mediated, CREB-mediated and steroid receptor-mediated transcription. Mutations in this gene cause Floating-Harbor syndrome, a rare disorder characterized by short stature, language deficits and dysmorphic facial features. [provided by RefSeq, Feb 2012]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BP6: Variant 16-30703955-A-C is Benign according to our data. Variant chr16-30703955-A-C is described in ClinVar as [Benign]. Clinvar id is 1304897.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.101 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
SRCAP	NM_006662.3	c.55-109A>C		intron_variant		ENST00000262518.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
SRCAP	ENST00000262518.9	c.55-109A>C		intron_variant		2	NM_006662.3	P1
SRCAP	ENST00000411466.7	c.55-109A>C		intron_variant		3		P1
SRCAP	ENST00000706321.1	c.55-109A>C		intron_variant				P1

Frequencies

GnomAD3 genomes AF: 0.0290 AC: 4414 AN: 152186 Hom.: 184 Cov.: 32

Gnomad AFR AF: 0.103

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00556

Gnomad ASJ AF: 0.00115

Gnomad EAS AF: 0.000384

Gnomad SAS AF: 0.000413

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.000220

Gnomad OTH AF: 0.0182

GnomAD4 exome AF: 0.00293 AC: 3430 AN: 1170250 Hom.: 164 AF XY: 0.00253 AC XY: 1467 AN XY: 579338

Gnomad4 AFR exome AF: 0.109

Gnomad4 AMR exome AF: 0.00531

Gnomad4 ASJ exome AF: 0.00167

Gnomad4 EAS exome AF: 0.00121

Gnomad4 SAS exome AF: 0.000173

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 0.0000914

Gnomad4 OTH exome AF: 0.00552

GnomAD4 genome AF: 0.0292 AC: 4444 AN: 152304 Hom.: 190 Cov.: 32 AF XY: 0.0283 AC XY: 2107 AN XY: 74486

Gnomad4 AFR AF: 0.104

Gnomad4 AMR AF: 0.00549

Gnomad4 ASJ AF: 0.00115

Gnomad4 EAS AF: 0.000385

Gnomad4 SAS AF: 0.00

Gnomad4 FIN AF: 0.00

Gnomad4 NFE AF: 0.000220

Gnomad4 OTH AF: 0.0180

Alfa AF: 0.00639 Hom.: 3

Bravo AF: 0.0330

Asia WGS AF: 0.00953 AC: 34 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Jul 23, 2021

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
Cadd	Benign	0.34
Dann	Benign	0.26

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs56209507; hg19: chr16-30715276;