chrY-12786501-C-CTT

Variant names:

• chrY-12786501-C-CTT
• rs149106583
• NM_004654.4:c.3283-6_3283-5dupTT

Variant summary

Our verdict is Likely benign. The variant received -4 ACMG points: 0P and 4B. BS2

The NM_004654.4(USP9Y):​c.3283-6_3283-5dupTT variant causes a splice region, 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: not found (cov: 0)
  • Exomes 𝑓: 0.0000067 (0 hom. 2 hem.)
• Consequence: USP9Y NM_004654.4 splice_region, intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.97
• Publications: 0 publications found

Genes affected

USP9Y (HGNC:12633): (ubiquitin specific peptidase 9 Y-linked) This gene is a member of the peptidase C19 family. It encodes a protein that is similar to ubiquitin-specific proteases, which cleave the ubiquitin moiety from ubiquitin-fused precursors and ubiquitinylated proteins. [provided by RefSeq, Mar 2009]

ACMG classification

Our verdict: Likely_benign. The variant received -4 ACMG points.

• BS2: High Hemizygotes in GnomAdExome4 at 2 YL gene

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_004654.4. 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
	USP9Y	NM_004654.4	MANE Select	c.3283-6_3283-5dupTT		splice_region intron	N/A	NP_004645.2	O00507-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	USP9Y	ENST00000338981.7	TSL:1 MANE Select	c.3283-21_3283-20insTT		intron	N/A	ENSP00000342812.3	O00507-1
	USP9Y	ENST00000651177.1		c.3283-21_3283-20insTT		intron	N/A	ENSP00000498372.1	O00507-1
	USP9Y	ENST00000857541.1		c.3283-21_3283-20insTT		intron	N/A	ENSP00000527600.1

Frequencies

GnomAD3 genomes Cov.: 0

GnomAD2 exomes AF: 0.00428 AC: 5 AN: 1167 AF XY: 0.00428

Gnomad AFR exome AF: 0.00

Gnomad AMR exome AF: 0.00

Gnomad ASJ exome AF: 0.00

Gnomad EAS exome AF: 0.00

Gnomad FIN exome AF: 0.00

Gnomad NFE exome AF: 0.00499

Gnomad OTH exome AF: 0.00

GnomAD4 exome AF: 0.00000672 AC: 2 AN: 297742 Hom.: 0 Cov.: 0 AF XY: 0.00000672 AC XY: 2 AN XY: 297742

African (AFR) AF: 0.00 AC: 0 AN: 5540

American (AMR) AF: 0.00 AC: 0 AN: 7298

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 5616

East Asian (EAS) AF: 0.00 AC: 0 AN: 8161

South Asian (SAS) AF: 0.0000771 AC: 2 AN: 25924

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 9502

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 1123

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 222686

Other (OTH) AF: 0.00 AC: 0 AN: 11892

GnomAD4 genome Cov.: 0

Alfa AF: 0.0657 Hom.: 57

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		-3.0

Splicing

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

Other links and lift over

dbSNP: rs149106583; hg19: chrY-14898435;