chr4-7218206-T-G

Variant names:

• chr4-7218206-T-G
• rs4234798
• NM_020777.3:c.480+25080T>G

Variant summary

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

The NM_020777.3(SORCS2):​c.480+25080T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.648 in 152,044 control chromosomes in the GnomAD database, including 32,076 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 0.65 (32076 hom., cov: 32)
• Consequence: SORCS2 NM_020777.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.18
• Publications: 31 publications found

Genes affected

SORCS2 (HGNC:16698): (sortilin related VPS10 domain containing receptor 2) This gene encodes one family member of vacuolar protein sorting 10 (VPS10) domain-containing receptor proteins. The VPS10 domain name comes from the yeast carboxypeptidase Y sorting receptor Vps10 protein. Members of this gene family are large with many exons but the CDS lengths are usually less than 3700 nt. Very large introns typically separate the exons encoding the VPS10 domain; the remaining exons are separated by much smaller-sized introns. These genes are strongly expressed in the central nervous system. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.708 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_020777.3. 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
	SORCS2	NM_020777.3	MANE Select	c.480+25080T>G		intron	N/A	NP_065828.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SORCS2	ENST00000507866.6	TSL:1 MANE Select	c.480+25080T>G		intron	N/A	ENSP00000422185.2

Frequencies

GnomAD3 genomes AF: 0.648 AC: 98432 AN: 151926 Hom.: 32043 Cov.: 32

Gnomad AFR AF: 0.712

Gnomad AMI AF: 0.689

Gnomad AMR AF: 0.636

Gnomad ASJ AF: 0.643

Gnomad EAS AF: 0.728

Gnomad SAS AF: 0.630

Gnomad FIN AF: 0.626

Gnomad MID AF: 0.564

Gnomad NFE AF: 0.610

Gnomad OTH AF: 0.654

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

GnomAD4 genome AF: 0.648 AC: 98521 AN: 152044 Hom.: 32076 Cov.: 32 AF XY: 0.648 AC XY: 48199 AN XY: 74328

African (AFR) AF: 0.712 AC: 29531 AN: 41480

American (AMR) AF: 0.636 AC: 9729 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.643 AC: 2225 AN: 3462

East Asian (EAS) AF: 0.727 AC: 3757 AN: 5166

South Asian (SAS) AF: 0.631 AC: 3036 AN: 4812

European-Finnish (FIN) AF: 0.626 AC: 6620 AN: 10570

Middle Eastern (MID) AF: 0.555 AC: 161 AN: 290

European-Non Finnish (NFE) AF: 0.610 AC: 41463 AN: 67958

Other (OTH) AF: 0.651 AC: 1372 AN: 2106

Alfa AF: 0.623 Hom.: 87808

Bravo AF: 0.655

Asia WGS AF: 0.706 AC: 2456 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	9.0
DANN	Benign	0.53
PhyloP100		1.2
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		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: rs4234798; hg19: chr4-7219933;