NM_001081573.3:c.1069+5811_1069+5813delTTT

Variant names:

• chrX-154706415-CAAA-C
• rs35975601
• NM_001081573.3:c.1069+5811_1069+5813delTTT

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 0P and 0B.

The NM_001081573.3(GAB3):​c.1069+5811_1069+5813delTTT variant causes a intron change involving the alteration of a non-conserved nucleotide. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.000011 (0 hom., 0 hem., cov: 0)
• Consequence: GAB3 NM_001081573.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.193
• Publications: 1 publications found

Genes affected

GAB3 (HGNC:17515): (GRB2 associated binding protein 3) This gene is a member of the GRB2-associated binding protein gene family. These proteins are scaffolding/docking proteins that are involved in several growth factor and cytokine signaling pathways, and they contain a pleckstrin homology domain, and bind SHP2 tyrosine phosphatase and GRB2 adapter protein. The protein encoded by this gene facilitates macrophage differentiation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
GAB3	NM_001081573.3	c.1069+5811_1069+5813delTTT		intron_variant	Intron 4 of 9	ENST00000424127.3	NP_001075042.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
GAB3	ENST00000424127.3	c.1069+5811_1069+5813delTTT		intron_variant	Intron 4 of 9	1	NM_001081573.3	ENSP00000399588.2
GAB3	ENST00000369575.7	c.1066+5811_1066+5813delTTT		intron_variant	Intron 4 of 9	1		ENSP00000358588.3
GAB3	ENST00000496390.5	n.617-6359_617-6357delTTT		intron_variant	Intron 3 of 8	1
GAB3	ENST00000369568.8	c.1069+5811_1069+5813delTTT		intron_variant	Intron 4 of 8	2		ENSP00000358581.4

Frequencies

GnomAD3 genomes AF: 0.0000107 AC: 1 AN: 93543 Hom.: 0 Cov.: 0

Gnomad AFR AF: 0.00

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.0000211

Gnomad OTH AF: 0.00

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

GnomAD4 genome AF: 0.0000107 AC: 1 AN: 93543 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 20595

⚠️ The allele balance in gnomAD version 4 Genomes is significantly skewed from the expected value of 0.5.

African (AFR) AF: 0.00 AC: 0 AN: 24731

American (AMR) AF: 0.00 AC: 0 AN: 8549

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 2386

East Asian (EAS) AF: 0.00 AC: 0 AN: 3045

South Asian (SAS) AF: 0.00 AC: 0 AN: 2014

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 3430

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 205

European-Non Finnish (NFE) AF: 0.0000211 AC: 1 AN: 47345

Other (OTH) AF: 0.00 AC: 0 AN: 1235

⚠️ The allele balance in gnomAD version 4 Genomes is significantly skewed from the expected value of 0.5. (p-value = 0), which strongly suggests a high chance of mosaicism in these individuals.

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
PhyloP100		0.19

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

Other links and lift over

dbSNP: rs35975601; hg19: chrX-153934690;