18-74496175-G-A

Variant names:

• chr18-74496175-G-A
• rs12964619
• ENST00000581272.5:c.-38+252G>A

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000581272.5(CNDP2):​c.-38+252G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.243 in 152,350 control chromosomes in the GnomAD database, including 4,815 homozygotes. 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: 𝑓 0.24 (4809 hom., cov: 34)
  • Exomes 𝑓: 0.28 (6 hom.)
• Consequence: CNDP2 ENST00000581272.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.165
• Publications: 10 publications found

Genes affected

CNDP2 (HGNC:24437): (carnosine dipeptidase 2) CNDP2, also known as tissue carnosinase and peptidase A (EC 3.4.13.18), is a nonspecific dipeptidase rather than a selective carnosinase (Teufel et al., 2003 [PubMed 12473676]).[supplied by OMIM, Mar 2008]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.06).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.316 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000581272.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CNDP2	NM_018235.3	MANE Select	c.-349G>A		upstream_gene	N/A	NP_060705.2
	CNDP2	NM_001370248.1		c.-294G>A		upstream_gene	N/A	NP_001357177.1
	CNDP2	NM_001370249.1		c.-616G>A		upstream_gene	N/A	NP_001357178.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CNDP2	ENST00000581272.5	TSL:4	c.-38+252G>A		intron	N/A	ENSP00000464151.1
	CNDP2	ENST00000324262.9	TSL:1 MANE Select	c.-349G>A		upstream_gene	N/A	ENSP00000325548.4
	CNDP2	ENST00000579847.5	TSL:5	c.-294G>A		upstream_gene	N/A	ENSP00000462311.1

Frequencies

GnomAD3 genomes AF: 0.243 AC: 36943 AN: 152080 Hom.: 4802 Cov.: 34

Gnomad AFR AF: 0.153

Gnomad AMI AF: 0.147

Gnomad AMR AF: 0.323

Gnomad ASJ AF: 0.209

Gnomad EAS AF: 0.297

Gnomad SAS AF: 0.300

Gnomad FIN AF: 0.244

Gnomad MID AF: 0.244

Gnomad NFE AF: 0.274

Gnomad OTH AF: 0.258

GnomAD4 exome AF: 0.283 AC: 43 AN: 152 Hom.: 6 Cov.: 0 AF XY: 0.281 AC XY: 32 AN XY: 114

African (AFR) AC: 0 AN: 0

American (AMR) AF: 0.00 AC: 0 AN: 2

Ashkenazi Jewish (ASJ) AF: 0.500 AC: 1 AN: 2

East Asian (EAS) AC: 0 AN: 0

South Asian (SAS) AF: 0.500 AC: 2 AN: 4

European-Finnish (FIN) AF: 0.125 AC: 1 AN: 8

Middle Eastern (MID) AC: 0 AN: 0

European-Non Finnish (NFE) AF: 0.276 AC: 32 AN: 116

Other (OTH) AF: 0.350 AC: 7 AN: 20

GnomAD4 genome AF: 0.243 AC: 36964 AN: 152198 Hom.: 4809 Cov.: 34 AF XY: 0.244 AC XY: 18189 AN XY: 74424

African (AFR) AF: 0.153 AC: 6343 AN: 41538

American (AMR) AF: 0.324 AC: 4955 AN: 15300

Ashkenazi Jewish (ASJ) AF: 0.209 AC: 727 AN: 3472

East Asian (EAS) AF: 0.297 AC: 1532 AN: 5162

South Asian (SAS) AF: 0.299 AC: 1444 AN: 4826

European-Finnish (FIN) AF: 0.244 AC: 2593 AN: 10612

Middle Eastern (MID) AF: 0.245 AC: 72 AN: 294

European-Non Finnish (NFE) AF: 0.274 AC: 18618 AN: 67972

Other (OTH) AF: 0.259 AC: 546 AN: 2112

Alfa AF: 0.266 Hom.: 2133

Bravo AF: 0.242

Asia WGS AF: 0.324 AC: 1130 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.1
CADD	Benign	6.4
DANN	Benign	0.87
PhyloP100		0.17
PromoterAI		0.021	Neutral

Splicing

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

Other links and lift over

dbSNP: rs12964619; hg19: chr18-72163410;