17-40140772-C-G

Variant names:

• chr17-40140772-C-G
• rs1315065108
• NM_007359.5:c.224C>G

Variant summary

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

The NM_007359.5(CASC3):​c.224C>G​(p.Ser75Trp) variant causes a missense change. The variant allele was found at a frequency of 0.00000584 in 1,027,596 control chromosomes in the GnomAD database, with no homozygous occurrence. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. S75L) has been classified as Uncertain significance.

• Frequency:
  • Genomes: not found (cov: 21)
  • Exomes 𝑓: 0.0000058 (0 hom.)
• Consequence: CASC3 NM_007359.5 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 4.96
• Publications: 0 publications found

Genes affected

CASC3 (HGNC:17040): (CASC3 exon junction complex subunit) The product of this gene is a core component of the exon junction complex (EJC), a protein complex that is deposited on spliced mRNAs at exon-exon junctions and functions in nonsense-mediated mRNA decay (NMD). The encoded protein binds RNA and interacts with two other EJC core components. It is predominantly located in the cytoplasm, but shuttles into the nucleus where it localizes to nuclear speckles. [provided by RefSeq, Jul 2008]

ENSG00000310351 (HGNC:):

ACMG classification

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

• BS2: High AC in GnomAdExome4 at 6 AD gene.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_007359.5. 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
	CASC3	NM_007359.5	MANE Select	c.224C>G	p.Ser75Trp	missense	Exon 1 of 14	NP_031385.2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CASC3	ENST00000264645.12	TSL:1 MANE Select	c.224C>G	p.Ser75Trp	missense	Exon 1 of 14	ENSP00000264645.6	O15234
	CASC3	ENST00000418132.7	TSL:1	n.455C>G		non_coding_transcript_exon	Exon 1 of 8
	CASC3	ENST00000971362.1		c.224C>G	p.Ser75Trp	missense	Exon 1 of 14	ENSP00000641421.1

Frequencies

GnomAD3 genomes Cov.: 21

GnomAD4 exome AF: 0.00000584 AC: 6 AN: 1027596 Hom.: 0 Cov.: 33 AF XY: 0.00000810 AC XY: 4 AN XY: 493848

African (AFR) AF: 0.0000475 AC: 1 AN: 21070

American (AMR) AF: 0.00 AC: 0 AN: 17334

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 10666

East Asian (EAS) AF: 0.00 AC: 0 AN: 10294

South Asian (SAS) AF: 0.00 AC: 0 AN: 56002

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 20834

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 2298

European-Non Finnish (NFE) AF: 0.00000586 AC: 5 AN: 853592

Other (OTH) AF: 0.00 AC: 0 AN: 35506

GnomAD4 genome Cov.: 21

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.91
BayesDel_addAF	Uncertain	0.094	D
BayesDel_noAF	Benign	-0.10
CADD	Pathogenic	32
DANN	Uncertain	0.99
DEOGEN2	Benign	0.27	T
Eigen	Uncertain	0.58
Eigen_PC	Uncertain	0.58
FATHMM_MKL	Benign	0.74	D
LIST_S2	Uncertain	0.89	D
M_CAP	Pathogenic	0.76	D
MetaRNN	Uncertain	0.60	D
MetaSVM	Benign	-0.50	T
MutationAssessor	Benign	1.1	L
PhyloP100		5.0
PrimateAI	Pathogenic	0.86	D
PROVEAN	Uncertain	-2.5	N
REVEL	Benign	0.16
Sift	Pathogenic	0.0	D
Sift4G	Pathogenic	0.0	D
Polyphen		1.0	D
Vest4		0.54
MutPred		0.19		Loss of phosphorylation at S75 (P = 0.0017)
MVP		0.42
MPC		2.1
ClinPred		1.0	D
GERP RS		4.9
PromoterAI		-0.081	Neutral
Varity_R		0.63
gMVP		0.36
Mutation Taster		=75/25	polymorphism

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.040		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: rs1315065108; hg19: chr17-38297025;