Genetic Variant VIPR1:c.637-725C>T (chr3-42530054-C-T) – ACMG Classification: Benign (-12 pts)

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_StrongBA1

The NM_004624.4(VIPR1):c.637-725C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.41 in 149,634 control chromosomes in the GnomAD database, including 12,880 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 0.41 ( 12863 hom., cov: 32)

Exomes 𝑓: 0.34 ( 17 hom. )

Consequence

VIPR1
NM_004624.4 intron

Scores

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 1.40

Publications

7 publications found

Variant links:

Genes affected

VIPR1 (HGNC:12694): (vasoactive intestinal peptide receptor 1) This gene encodes a receptor for vasoactive intestinal peptide, a small neuropeptide. Vasoactive intestinal peptide is involved in smooth muscle relaxation, exocrine and endocrine secretion, and water and ion flux in lung and intestinal epithelia. Its actions are effected through integral membrane receptors associated with a guanine nucleotide binding protein which activates adenylate cyclase. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]

VIPR1 links:

VIPR1-AS1 (HGNC:40610): (VIPR1 antisense RNA 1)

VIPR1-AS1 links:

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ACMG classification

Classification was made for transcript

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

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.8).

BA1

GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.553 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_004624.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Gene	Transcript	Tags	HGVSc	Effect	Exon Rank	Protein	UniProt
VIPR1	NM_004624.4	MANE Select	c.637-725C>T	intron	N/A	NP_004615.2
VIPR1	NM_001251885.2		c.556-725C>T	intron	N/A	NP_001238814.1	B4DNY6
VIPR1	NM_001251882.2		c.514-725C>T	intron	N/A	NP_001238811.1	P32241-5

Ensembl Transcripts

Gene	Transcript	Tags	HGVSc	Effect	Exon Rank	Protein	UniProt
VIPR1	ENST00000325123.5	TSL:1 MANE Select	c.637-725C>T	intron	N/A	ENSP00000327246.4	P32241-1
VIPR1	ENST00000883021.1		c.667-725C>T	intron	N/A	ENSP00000553080.1
VIPR1	ENST00000883016.1		c.634-725C>T	intron	N/A	ENSP00000553075.1

Frequencies

GnomAD3 genomes

AF:

0.411

AC:

61268

AN:

149218

Hom.:

12865

Cov.:

show subpopulations

Gnomad AFR

AF:

0.291

Gnomad AMI

AF:

0.348

Gnomad AMR

AF:

0.444

Gnomad ASJ

AF:

0.516

Gnomad EAS

AF:

0.571

Gnomad SAS

AF:

0.542

Gnomad FIN

AF:

0.449

Gnomad MID

AF:

0.487

Gnomad NFE

AF:

0.440

Gnomad OTH

AF:

0.425

GnomAD4 exome

AF:

0.338

AC:

100

AN:

296

Hom.:

Cov.:

AF XY:

0.298

AC XY:

AN XY:

168

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

American (AMR)

AF:

0.222

AC:

AN:

Ashkenazi Jewish (ASJ)

AC:

AN:

East Asian (EAS)

AC:

AN:

South Asian (SAS)

AF:

0.333

AC:

AN:

European-Finnish (FIN)

AF:

0.438

AC:

AN:

Middle Eastern (MID)

AC:

AN:

European-Non Finnish (NFE)

AF:

0.333

AC:

AN:

204

Other (OTH)

AF:

0.313

AC:

AN:

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.527

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Exome Hom

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

AF:

0.410

AC:

61284

AN:

149338

Hom.:

12863

Cov.:

AF XY:

0.413

AC XY:

30116

AN XY:

72938

show subpopulations

African (AFR)

AF:

0.291

AC:

11440

AN:

39302

American (AMR)

AF:

0.444

AC:

6750

AN:

15210

Ashkenazi Jewish (ASJ)

AF:

0.516

AC:

1786

AN:

3458

East Asian (EAS)

AF:

0.571

AC:

2862

AN:

5016

South Asian (SAS)

AF:

0.542

AC:

2572

AN:

4746

European-Finnish (FIN)

AF:

0.449

AC:

4700

AN:

10474

Middle Eastern (MID)

AF:

0.483

AC:

142

AN:

294

European-Non Finnish (NFE)

AF:

0.440

AC:

29834

AN:

67848

Other (OTH)

AF:

0.423

AC:

885

AN:

2090

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.500

Heterozygous variant carriers

1819

3639

5458

7278

9097

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome Het

Genome Hom

Variant carriers

590

1180

1770

2360

2950

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

Alfa

AF:

0.426

Hom.:

2812

Bravo

AF:

0.400

Asia WGS

AF:

0.521

AC:

1816

AN:

3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.80

CADD

Benign

5.4

(source)

DANN

Benign

0.34

PhyloP100

1.4

Mutation Taster

=100/0

polymorphism (auto)

(source)

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

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Variant Effect in Transcripts

RefSeq Transcripts

Ensembl Transcripts

Frequencies

Age Distribution

Age Distribution

ClinVar

Computational scores

Splicing

Publications

Other links and lift over