rs1894116

chr11-102199908-A-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001130145.3(YAP1):c.803-5985A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0841 in 152,304 control chromosomes in the GnomAD database, including 622 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 0.084 (622 hom., cov: 32)
• Consequence: YAP1 NM_001130145.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.14

Genes affected

YAP1 (HGNC:16262): (Yes1 associated transcriptional regulator) This gene encodes a downstream nuclear effector of the Hippo signaling pathway which is involved in development, growth, repair, and homeostasis. This gene is known to play a role in the development and progression of multiple cancers as a transcriptional regulator of this signaling pathway and may function as a potential target for cancer treatment. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2013]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.193 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
YAP1	NM_001130145.3	c.803-5985A>G		intron_variant		ENST00000282441.10

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
YAP1	ENST00000282441.10	c.803-5985A>G		intron_variant		1	NM_001130145.3	P2

Frequencies

GnomAD3 genomes AF: 0.0842 AC: 12819 AN: 152186 Hom.: 624 Cov.: 32

Gnomad AFR AF: 0.0808

Gnomad AMI AF: 0.0844

Gnomad AMR AF: 0.0477

Gnomad ASJ AF: 0.125

Gnomad EAS AF: 0.178

Gnomad SAS AF: 0.205

Gnomad FIN AF: 0.0504

Gnomad MID AF: 0.0828

Gnomad NFE AF: 0.0822

Gnomad OTH AF: 0.0774

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.0841 AC: 12815 AN: 152304 Hom.: 622 Cov.: 32 AF XY: 0.0858 AC XY: 6392 AN XY: 74472

Gnomad4 AFR AF: 0.0808

Gnomad4 AMR AF: 0.0476

Gnomad4 ASJ AF: 0.125

Gnomad4 EAS AF: 0.177

Gnomad4 SAS AF: 0.204

Gnomad4 FIN AF: 0.0504

Gnomad4 NFE AF: 0.0822

Gnomad4 OTH AF: 0.0770

Alfa AF: 0.0864 Hom.: 981

Bravo AF: 0.0813

Asia WGS AF: 0.168 AC: 585 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
Cadd	Benign	10
Dann	Benign	0.79

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: rs1894116; hg19: chr11-102070639;