rs767782509

Variant names:

• chr19-50943757-A-C
• rs767782509
• NM_012427.5:c.756T>G

Your query was ambiguous. Multiple possible variants found:

• chr19-50943757-A-C
• chr19-50943757-A-G
• chr19-50943757-A-T

Variant summary

Our verdict is Uncertain significance. Variant got 4 ACMG points: 4P and 0B. PM1 PM2

The NM_012427.5(KLK5):​c.756T>G​(p.Asn252Lys) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 13/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another nucleotide change resulting in the same amino acid substitution has been previously reported as Uncertain significance in ClinVar.

• Frequency: Genomes: not found (cov: 31)
• Consequence: KLK5 NM_012427.5 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.86

Genes affected

KLK5 (HGNC:6366): (kallikrein related peptidase 5) Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Its expression is up-regulated by estrogens and progestins. The encoded protein is secreted and may be involved in desquamation in the epidermis. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 4 ACMG points.

• PM1: In a glycosylation_site N-linked (GlcNAc...) asparagine (size 0) in uniprot entity KLK5_HUMAN
• PM2: Very rare variant in population databases, with high coverage

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
KLK5	NM_012427.5	c.756T>G	p.Asn252Lys	missense_variant	Exon 6 of 6	ENST00000336334.8	NP_036559.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
KLK5	ENST00000336334.8	c.756T>G	p.Asn252Lys	missense_variant	Exon 6 of 6	1	NM_012427.5	ENSP00000337733.2
KLK5	ENST00000391809.6	c.756T>G	p.Asn252Lys	missense_variant	Exon 7 of 7	1		ENSP00000375685.1
KLK5	ENST00000593428.5	c.756T>G	p.Asn252Lys	missense_variant	Exon 6 of 6	1		ENSP00000471966.1
KLK5	ENST00000595585.1	n.852T>G		non_coding_transcript_exon_variant	Exon 4 of 4	2

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 31

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.23
BayesDel_addAF	Benign	-0.082	T
BayesDel_noAF	Benign	-0.36
CADD	Benign	0.042
DANN	Benign	0.97
DEOGEN2	Uncertain	0.66	D;D;D
Eigen	Benign	-1.0
Eigen_PC	Benign	-1.0
FATHMM_MKL	Benign	0.12	N
LIST_S2	Benign	0.41	.;.;T
M_CAP	Benign	0.046	D
MetaRNN	Uncertain	0.58	D;D;D
MetaSVM	Benign	-0.49	T
MutationAssessor	Benign	1.3	L;L;L
PrimateAI	Uncertain	0.48	T
PROVEAN	Uncertain	-4.0	D;D;.
REVEL	Benign	0.18
Sift	Benign	0.049	D;D;.
Sift4G	Benign	0.22	T;T;T
Polyphen		0.099	B;B;B
Vest4		0.52
MutPred		0.66		Gain of methylation at N252 (P = 0);Gain of methylation at N252 (P = 0);Gain of methylation at N252 (P = 0);
MVP		0.80
MPC		0.11
ClinPred		0.13	T
GERP RS		1.3
Varity_R		0.25
gMVP		0.67

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

Publications

LitVar

Other links and lift over

dbSNP: rs767782509; hg19: chr19-51447013;