rs6779719

Variant names:

• chr3-4837700-G-A
• rs6779719
• NM_001378452.1:c.8190+765G>A

Your query was ambiguous. Multiple possible variants found:

• chr3-4837700-G-A
• chr3-4837700-G-C
• chr3-4837700-G-T

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001378452.1(ITPR1):​c.8190+765G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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: not found (cov: 30)
• Consequence: ITPR1 NM_001378452.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.944
• Publications: 0 publications found

Genes affected

ITPR1 (HGNC:6180): (inositol 1,4,5-trisphosphate receptor type 1) This gene encodes an intracellular receptor for inositol 1,4,5-trisphosphate. Upon stimulation by inositol 1,4,5-trisphosphate, this receptor mediates calcium release from the endoplasmic reticulum. Mutations in this gene cause spinocerebellar ataxia type 15, a disease associated with an heterogeneous group of cerebellar disorders. Multiple transcript variants have been identified for this gene. [provided by RefSeq, Nov 2009]

ITPR1 Gene-Disease associations (from GenCC):

• aniridia-cerebellar ataxia-intellectual disability syndrome

  Inheritance: AD, AR Classification: DEFINITIVE, STRONG, MODERATE, SUPPORTIVE Submitted by: Ambry Genetics, G2P, Genomics England PanelApp, PanelApp Australia, Labcorp Genetics (formerly Invitae), Orphanet, ClinGen
• spinocerebellar ataxia type 29

  Inheritance: AD Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Labcorp Genetics (formerly Invitae), G2P, ClinGen, Orphanet
• spinocerebellar ataxia type 15/16

  Inheritance: AD Classification: STRONG, SUPPORTIVE Submitted by: Orphanet, Labcorp Genetics (formerly Invitae)

ENSG00000235978 (HGNC:):

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ITPR1	NM_001378452.1	c.8190+765G>A		intron_variant	Intron 61 of 61	ENST00000649015.2	NP_001365381.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ITPR1	ENST00000649015.2	c.8190+765G>A		intron_variant	Intron 61 of 61		NM_001378452.1	ENSP00000497605.1
ITPR1	ENST00000354582.12	c.8166+765G>A		intron_variant	Intron 61 of 61	5		ENSP00000346595.8
ITPR1	ENST00000648266.1	c.8163+765G>A		intron_variant	Intron 61 of 61			ENSP00000498014.1
ITPR1	ENST00000650294.1	c.8148+765G>A		intron_variant	Intron 60 of 60			ENSP00000498056.1
ITPR1	ENST00000443694.5	c.8145+765G>A		intron_variant	Intron 60 of 60	1		ENSP00000401671.2
ITPR1	ENST00000648309.1	c.8118+765G>A		intron_variant	Intron 58 of 58			ENSP00000497026.1
ITPR1	ENST00000357086.10	c.8046+765G>A		intron_variant	Intron 58 of 58	1		ENSP00000349597.4
ITPR1	ENST00000456211.8	c.8001+765G>A		intron_variant	Intron 57 of 57	1		ENSP00000397885.2
ITPR1	ENST00000648038.1	c.5952+765G>A		intron_variant	Intron 41 of 41			ENSP00000497872.1
ITPR1	ENST00000648431.1	c.5367+765G>A		intron_variant	Intron 38 of 38			ENSP00000498149.1
ITPR1	ENST00000648212.1	c.5130+765G>A		intron_variant	Intron 38 of 38			ENSP00000498022.1

Frequencies

GnomAD3 genomes Cov.: 30

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

GnomAD4 genome Cov.: 30

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.28
DANN	Benign	0.95
PhyloP100		-0.94

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: rs6779719; hg19: chr3-4879384;