rs4918255

Variant names:

• chr10-106804960-T-C
• rs4918255
• NM_052918.5:c.726+24614A>G

Your query was ambiguous. Multiple possible variants found:

• chr10-106804960-T-C
• chr10-106804960-T-G

Variant summary

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

The NM_052918.5(SORCS1):​c.726+24614A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.29 in 152,036 control chromosomes in the GnomAD database, including 6,556 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 0.29 (6556 hom., cov: 32)
• Consequence: SORCS1 NM_052918.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.220
• Publications: 5 publications found

Genes affected

SORCS1 (HGNC:16697): (sortilin related VPS10 domain containing receptor 1) 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. Two of the five family members (sortilin and sortilin-related receptor) are synthesized as preproproteins; it is not yet known if this encoded protein is also a preproprotein. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

SORCS1 Gene-Disease associations (from GenCC):

• schizophrenia

  Inheritance: Unknown Classification: NO_KNOWN Submitted by: Labcorp Genetics (formerly Invitae)

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 (NFE) allele frequency at 95% confidence interval = 0.307 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_052918.5. 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
	SORCS1	NM_052918.5	MANE Select	c.726+24614A>G		intron	N/A	NP_443150.3
	SORCS1	NM_001387556.1		c.726+24614A>G		intron	N/A	NP_001374485.1
	SORCS1	NM_001013031.3		c.726+24614A>G		intron	N/A	NP_001013049.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SORCS1	ENST00000263054.11	TSL:1 MANE Select	c.726+24614A>G		intron	N/A	ENSP00000263054.5

Frequencies

GnomAD3 genomes AF: 0.289 AC: 43967 AN: 151918 Hom.: 6540 Cov.: 32

Gnomad AFR AF: 0.305

Gnomad AMI AF: 0.419

Gnomad AMR AF: 0.255

Gnomad ASJ AF: 0.224

Gnomad EAS AF: 0.105

Gnomad SAS AF: 0.192

Gnomad FIN AF: 0.296

Gnomad MID AF: 0.187

Gnomad NFE AF: 0.311

Gnomad OTH AF: 0.260

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

GnomAD4 genome AF: 0.290 AC: 44038 AN: 152036 Hom.: 6556 Cov.: 32 AF XY: 0.286 AC XY: 21254 AN XY: 74314

African (AFR) AF: 0.305 AC: 12675 AN: 41500

American (AMR) AF: 0.255 AC: 3893 AN: 15270

Ashkenazi Jewish (ASJ) AF: 0.224 AC: 776 AN: 3470

East Asian (EAS) AF: 0.105 AC: 545 AN: 5186

South Asian (SAS) AF: 0.191 AC: 919 AN: 4820

European-Finnish (FIN) AF: 0.296 AC: 3130 AN: 10558

Middle Eastern (MID) AF: 0.211 AC: 62 AN: 294

European-Non Finnish (NFE) AF: 0.311 AC: 21102 AN: 67922

Other (OTH) AF: 0.264 AC: 556 AN: 2108

Alfa AF: 0.297 Hom.: 30154

Bravo AF: 0.289

Asia WGS AF: 0.179 AC: 624 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	3.8
DANN	Benign	0.81
PhyloP100		0.22
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: rs4918255; hg19: chr10-108564718;