10-112747837-G-C

Variant names:

• chr10-112747837-G-C
• rs7070850
• NM_145206.4:c.561-67453G>C

Variant summary

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

The NM_145206.4(VTI1A):​c.561-67453G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.331 in 152,024 control chromosomes in the GnomAD database, including 9,044 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 0.33 (9044 hom., cov: 32)
• Consequence: VTI1A NM_145206.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.259
• Publications: 1 publications found

Genes affected

VTI1A (HGNC:17792): (vesicle transport through interaction with t-SNAREs 1A) The protein encoded by this gene is a member of the family of soluble N-ethylmaleimide-sensitive fusion protein-attachment protein receptors (SNAREs) that function in intracellular trafficking. This family member is involved in vesicular transport between endosomes and the trans-Golgi network. It is a vesicle-associated SNARE (v-SNARE) that interacts with target membrane SNAREs (t-SNAREs). Polymorphisms in this gene have been associated with binocular function, and also with susceptibility to colorectal and lung cancers. A recurrent rearrangement has been found between this gene and the transcription factor 7-like 2 (TCF7L2) gene in colorectal cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.472 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
VTI1A	NM_145206.4	c.561-67453G>C		intron_variant	Intron 7 of 7	ENST00000393077.3	NP_660207.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
VTI1A	ENST00000393077.3	c.561-67453G>C		intron_variant	Intron 7 of 7	2	NM_145206.4	ENSP00000376792.2
VTI1A	ENST00000705995.1	c.582-67453G>C		intron_variant	Intron 8 of 8			ENSP00000516199.1

Frequencies

GnomAD3 genomes AF: 0.331 AC: 50237 AN: 151906 Hom.: 9035 Cov.: 32

Gnomad AFR AF: 0.478

Gnomad AMI AF: 0.126

Gnomad AMR AF: 0.312

Gnomad ASJ AF: 0.344

Gnomad EAS AF: 0.419

Gnomad SAS AF: 0.227

Gnomad FIN AF: 0.192

Gnomad MID AF: 0.304

Gnomad NFE AF: 0.270

Gnomad OTH AF: 0.337

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

GnomAD4 genome AF: 0.331 AC: 50286 AN: 152024 Hom.: 9044 Cov.: 32 AF XY: 0.327 AC XY: 24286 AN XY: 74326

African (AFR) AF: 0.478 AC: 19789 AN: 41434

American (AMR) AF: 0.313 AC: 4779 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.344 AC: 1195 AN: 3472

East Asian (EAS) AF: 0.418 AC: 2158 AN: 5164

South Asian (SAS) AF: 0.226 AC: 1087 AN: 4808

European-Finnish (FIN) AF: 0.192 AC: 2036 AN: 10584

Middle Eastern (MID) AF: 0.286 AC: 84 AN: 294

European-Non Finnish (NFE) AF: 0.270 AC: 18336 AN: 67972

Other (OTH) AF: 0.336 AC: 708 AN: 2106

Alfa AF: 0.134 Hom.: 210

Bravo AF: 0.359

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.19
DANN	Benign	0.50
PhyloP100		-0.26
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: rs7070850; hg19: chr10-114507596;