rs772309606

Variant names:

• chr1-115659707-C-G
• rs772309606
• NM_138959.3:c.138C>G

Your query was ambiguous. Multiple possible variants found:

• chr1-115659707-C-G
• chr1-115659707-C-T

Variant summary

Our verdict is Likely benign. Variant got -1 ACMG points: 2P and 3B. PM2 BP4_Moderate BP7

The NM_138959.3(VANGL1):​c.138C>G​(p.Val46Val) variant causes a synonymous 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. Synonymous variant affecting the same amino acid position (i.e. V46V) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: VANGL1 NM_138959.3 synonymous
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 2.65

Genes affected

VANGL1 (HGNC:15512): (VANGL planar cell polarity protein 1) This gene encodes a member of the tretraspanin family. The encoded protein may be involved in mediating intestinal trefoil factor induced wound healing in the intestinal mucosa. Mutations in this gene are associated with neural tube defects. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]

ACMG classification

Verdict is Likely_benign. Variant got -1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.37).
• BP7: Synonymous conserved (PhyloP=2.65 with no splicing effect.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
VANGL1	NM_138959.3	c.138C>G	p.Val46Val	synonymous_variant	Exon 3 of 8	ENST00000355485.7	NP_620409.1
VANGL1	NM_001172412.2	c.138C>G	p.Val46Val	synonymous_variant	Exon 3 of 8		NP_001165883.1
VANGL1	NM_001172411.2	c.138C>G	p.Val46Val	synonymous_variant	Exon 3 of 8		NP_001165882.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
VANGL1	ENST00000355485.7	c.138C>G	p.Val46Val	synonymous_variant	Exon 3 of 8	1	NM_138959.3	ENSP00000347672.2
VANGL1	ENST00000310260.7	c.138C>G	p.Val46Val	synonymous_variant	Exon 3 of 8	1		ENSP00000310800.3
VANGL1	ENST00000369509.1	c.138C>G	p.Val46Val	synonymous_variant	Exon 2 of 7	1		ENSP00000358522.1
VANGL1	ENST00000369510.8	c.138C>G	p.Val46Val	synonymous_variant	Exon 3 of 8	1		ENSP00000358523.3

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD3 exomes AF: 0.00000398 AC: 1 AN: 251456 Hom.: 0 AF XY: 0.00 AC XY: 0 AN XY: 135896

Gnomad AFR exome AF: 0.00

Gnomad AMR exome AF: 0.00

Gnomad ASJ exome AF: 0.00

Gnomad EAS exome AF: 0.0000544

Gnomad SAS exome AF: 0.00

Gnomad FIN exome AF: 0.00

Gnomad NFE exome AF: 0.00

Gnomad OTH exome AF: 0.00

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 32

Bravo AF: 0.00000378

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.37
CADD	Benign	12
DANN	Benign	0.76
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7

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

Publications

LitVar

Other links and lift over

dbSNP: rs772309606; hg19: chr1-116202328;