rs2664156

Variant names:

• chr19-50873907-T-A
• rs2664156
• NM_005551.5:c.46+388T>A

Your query was ambiguous. Multiple possible variants found:

• chr19-50873907-T-A
• chr19-50873907-T-C
• chr19-50873907-T-G

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_005551.5(KLK2):​c.46+388T>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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: not found (cov: 30)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: KLK2 NM_005551.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -4.46
• Publications: 8 publications found

Genes affected

KLK2 (HGNC:6363): (kallikrein related peptidase 2) This gene encodes a member of the grandular kallikrein protein family. Kallikreins are a subgroup of serine proteases that are clustered on chromosome 19. Members of this family are involved in a diverse array of biological functions. The protein encoded by this gene is a highly active trypsin-like serine protease that selectively cleaves at arginine residues. This protein is primarily expressed in prostatic tissue and is responsible for cleaving pro-prostate-specific antigen into its enzymatically active form. This gene is highly expressed in prostate tumor cells and may be a prognostic maker for prostate cancer risk. Alternate splicing results in both coding and non-coding transcript variants. [provided by RefSeq, Jan 2012]

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
KLK2	NM_005551.5	c.46+388T>A		intron_variant	Intron 1 of 4	ENST00000325321.8	NP_005542.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
KLK2	ENST00000325321.8	c.46+388T>A		intron_variant	Intron 1 of 4	1	NM_005551.5	ENSP00000313581.2

Frequencies

GnomAD3 genomes Cov.: 30

GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 50770 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 25992

African (AFR) AF: 0.00 AC: 0 AN: 1516

American (AMR) AF: 0.00 AC: 0 AN: 2562

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 2004

East Asian (EAS) AF: 0.00 AC: 0 AN: 3172

South Asian (SAS) AF: 0.00 AC: 0 AN: 2396

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 2770

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 276

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 32722

Other (OTH) AF: 0.00 AC: 0 AN: 3352

GnomAD4 genome Cov.: 30

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	0.94
DANN	Benign	0.34
PhyloP100		-4.5
PromoterAI		0.0019	Neutral

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs2664156; hg19: chr19-51377163;