NM_001317938.2:c.114+2554C>G

Variant names:

• chr5-127710314-C-G
• rs248742
• NM_001317938.2:c.114+2554C>G

Variant summary

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

The NM_001317938.2(CCDC192):​c.114+2554C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.31 in 151,760 control chromosomes in the GnomAD database, including 7,614 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 0.31 (7614 hom., cov: 31)
• Consequence: CCDC192 NM_001317938.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.994
• Publications: 2 publications found

Genes affected

CCDC192 (HGNC:49566): (coiled-coil domain containing 192)

ENSG00000248799 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.413 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001317938.2. 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
	CCDC192	NM_001317938.2	MANE Select	c.114+2554C>G		intron	N/A	NP_001304867.2	A0A9S7N7Z0

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CCDC192	ENST00000514853.5	TSL:5 MANE Select	c.114+2554C>G		intron	N/A	ENSP00000490579.2	A0A9S7N7Z0
	CCDC192	ENST00000706942.1		c.171+2554C>G		intron	N/A	ENSP00000516662.1	P0DO97
	ENSG00000248799	ENST00000827054.1		n.95-915G>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.310 AC: 46975 AN: 151642 Hom.: 7610 Cov.: 31

Gnomad AFR AF: 0.221

Gnomad AMI AF: 0.323

Gnomad AMR AF: 0.373

Gnomad ASJ AF: 0.300

Gnomad EAS AF: 0.377

Gnomad SAS AF: 0.431

Gnomad FIN AF: 0.330

Gnomad MID AF: 0.259

Gnomad NFE AF: 0.333

Gnomad OTH AF: 0.323

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

GnomAD4 genome AF: 0.310 AC: 46985 AN: 151760 Hom.: 7614 Cov.: 31 AF XY: 0.313 AC XY: 23240 AN XY: 74166

African (AFR) AF: 0.220 AC: 9119 AN: 41358

American (AMR) AF: 0.374 AC: 5708 AN: 15268

Ashkenazi Jewish (ASJ) AF: 0.300 AC: 1042 AN: 3470

East Asian (EAS) AF: 0.377 AC: 1936 AN: 5138

South Asian (SAS) AF: 0.428 AC: 2055 AN: 4796

European-Finnish (FIN) AF: 0.330 AC: 3461 AN: 10500

Middle Eastern (MID) AF: 0.252 AC: 74 AN: 294

European-Non Finnish (NFE) AF: 0.333 AC: 22615 AN: 67920

Other (OTH) AF: 0.324 AC: 682 AN: 2108

Alfa AF: 0.184 Hom.: 402

Bravo AF: 0.310

Asia WGS AF: 0.392 AC: 1362 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	0.42
DANN	Benign	0.63
PhyloP100		-0.99

Splicing

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

Other links and lift over

dbSNP: rs248742; hg19: chr5-127046006;