NM_001017365.3:c.410-9T>C

Variant names:

• chr1-207096513-T-C
• rs3813948
• NM_001017365.3:c.410-9T>C

Variant summary

Our verdict is Benign. The variant received -20 ACMG points: 0P and 20B. BP4_Strong BP6_Very_Strong BA1

The NM_001017365.3(C4BPB):​c.410-9T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0785 in 1,554,250 control chromosomes in the GnomAD database, including 5,925 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.10 (965 hom., cov: 32)
  • Exomes 𝑓: 0.076 (4960 hom.)
• Consequence: C4BPB NM_001017365.3 intron
• Scores: Splicing: ADA: 0.00005132
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:3
• Conservation: PhyloP100: 0.124
• Publications: 46 publications found

Genes affected

C4BPB (HGNC:1328): (complement component 4 binding protein beta) This gene encodes a member of a superfamily of proteins composed predominantly of tandemly arrayed short consensus repeats of approximately 60 amino acids. A single, unique beta-chain encoded by this gene assembles with seven identical alpha-chains into the predominant isoform of C4b-binding protein, a multimeric protein that controls activation of the complement cascade through the classical pathway. C4b-binding protein has a regulatory role in the coagulation system also, mediated through the beta-chain binding of protein S, a vitamin K-dependent protein that serves as a cofactor of activated protein C. The genes encoding both alpha and beta chains are located adjacent to each other on human chromosome 1 in the regulator of complement activation gene cluster. Alternative splicing gives rise to multiple transcript variants. [provided by RefSeq, Jul 2008]

ACMG classification

Our verdict: Benign. The variant received -20 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BP6: Variant 1-207096513-T-C is Benign according to our data. Variant chr1-207096513-T-C is described in ClinVar as Benign. ClinVar VariationId is 402448.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.159 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001017365.3. 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
	C4BPB	NM_001017365.3	MANE Select	c.410-9T>C		intron	N/A	NP_001017365.1	P20851-1
	C4BPB	NM_000716.3		c.410-9T>C		intron	N/A	NP_000707.1	P20851-1
	C4BPB	NM_001017367.1		c.410-9T>C		intron	N/A	NP_001017367.1	P20851-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	C4BPB	ENST00000367078.8	TSL:1 MANE Select	c.410-9T>C		intron	N/A	ENSP00000356045.3	P20851-1
	C4BPB	ENST00000243611.9	TSL:1	c.410-9T>C		intron	N/A	ENSP00000243611.5	P20851-1
	C4BPB	ENST00000367076.7	TSL:1	c.407-9T>C		intron	N/A	ENSP00000356043.3	P20851-2

Frequencies

GnomAD3 genomes AF: 0.102 AC: 15556 AN: 152052 Hom.: 965 Cov.: 32

Gnomad AFR AF: 0.163

Gnomad AMI AF: 0.0789

Gnomad AMR AF: 0.0775

Gnomad ASJ AF: 0.121

Gnomad EAS AF: 0.164

Gnomad SAS AF: 0.124

Gnomad FIN AF: 0.0557

Gnomad MID AF: 0.187

Gnomad NFE AF: 0.0705

Gnomad OTH AF: 0.121

GnomAD2 exomes AF: 0.0912 AC: 22869 AN: 250852 AF XY: 0.0928

Gnomad AFR exome AF: 0.164

Gnomad AMR exome AF: 0.0518

Gnomad ASJ exome AF: 0.116

Gnomad EAS exome AF: 0.160

Gnomad FIN exome AF: 0.0564

Gnomad NFE exome AF: 0.0768

Gnomad OTH exome AF: 0.0985

GnomAD4 exome AF: 0.0760 AC: 106513 AN: 1402080 Hom.: 4960 Cov.: 25 AF XY: 0.0778 AC XY: 54586 AN XY: 701354

African (AFR) AF: 0.165 AC: 5092 AN: 30860

American (AMR) AF: 0.0543 AC: 2421 AN: 44588

Ashkenazi Jewish (ASJ) AF: 0.113 AC: 2907 AN: 25682

East Asian (EAS) AF: 0.176 AC: 6928 AN: 39322

South Asian (SAS) AF: 0.119 AC: 10077 AN: 84928

European-Finnish (FIN) AF: 0.0553 AC: 2950 AN: 53384

Middle Eastern (MID) AF: 0.184 AC: 1034 AN: 5612

European-Non Finnish (NFE) AF: 0.0659 AC: 69804 AN: 1059500

Other (OTH) AF: 0.0911 AC: 5300 AN: 58204

GnomAD4 genome AF: 0.102 AC: 15564 AN: 152170 Hom.: 965 Cov.: 32 AF XY: 0.101 AC XY: 7521 AN XY: 74408

African (AFR) AF: 0.163 AC: 6746 AN: 41500

American (AMR) AF: 0.0775 AC: 1184 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.121 AC: 421 AN: 3466

East Asian (EAS) AF: 0.165 AC: 852 AN: 5174

South Asian (SAS) AF: 0.124 AC: 599 AN: 4824

European-Finnish (FIN) AF: 0.0557 AC: 591 AN: 10604

Middle Eastern (MID) AF: 0.180 AC: 53 AN: 294

European-Non Finnish (NFE) AF: 0.0705 AC: 4795 AN: 68012

Other (OTH) AF: 0.119 AC: 251 AN: 2104

Alfa AF: 0.0822 Hom.: 2547

Bravo AF: 0.106

Asia WGS AF: 0.151 AC: 524 AN: 3478

EpiCase AF: 0.0808

EpiControl AF: 0.0824

ClinVar

ClinVar submissions as Germline

Significance: Benign

Revision: criteria provided, multiple submitters, no conflicts

Pathogenic	VUS	Benign	Condition
-	-	2	not provided (2)
-	-	1	not specified (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	1.5
DANN	Benign	0.64
PhyloP100		0.12
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
dbscSNV1_ADA	Benign	0.000051
dbscSNV1_RF	Benign	0.0
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: rs3813948; hg19: chr1-207269858;