rs756307171

Variant names:

• chr3-10117393-CTTTTTTTTTTT-C
• rs756307171
• NM_018462.5:c.118+1584_118+1594delTTTTTTTTTTT

Your query was ambiguous. Multiple possible variants found:

• chr3-10117393-CTTTTTTTTTTT-C
• chr3-10117393-CTTTTTTTTTTT-CTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTTTTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTTTTTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTTTTTTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTTTTTTTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTTTTTTTTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTTTTTTTTTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTTTTTTTTTTTTTT
• chr3-10117393-CTTTTTTTTTTT-CTTTTTTTTTTTTTTTTTTT

Variant summary

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

The NM_018462.5(BRK1):​c.118+1584_118+1594delTTTTTTTTTTT variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. It is difficult to determine the true allele frequency of this variant because it is of type DEL_BIG, and the frequency of such variant types in population databases may be underestimated and unreliable. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 21)
• Consequence: BRK1 NM_018462.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.754
• Publications: 0 publications found

Genes affected

BRK1 (HGNC:23057): (BRICK1 subunit of SCAR/WAVE actin nucleating complex) Enables identical protein binding activity. Contributes to small GTPase binding activity. Involved in Rac protein signal transduction and positive regulation of cellular component organization. Located in extracellular exosome. Part of SCAR complex. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_018462.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	BRK1	NM_018462.5	MANE Select	c.118+1584_118+1594delTTTTTTTTTTT		intron	N/A	NP_060932.2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	BRK1	ENST00000530758.2	TSL:1 MANE Select	c.118+1575_118+1585delTTTTTTTTTTT		intron	N/A	ENSP00000432472.1	Q8WUW1-1
	BRK1	ENST00000916415.1		c.114-1512_114-1502delTTTTTTTTTTT		intron	N/A	ENSP00000586474.1

Frequencies

GnomAD3 genomes Cov.: 21

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

GnomAD4 genome Cov.: 21

Alfa AF: 0.00 Hom.: 70

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		0.75

Splicing

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

Other links and lift over

dbSNP: rs756307171; hg19: chr3-10159077;