19-7747847-A-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_StrongBA1

The variant allele was found at a frequency of 0.253 in 152,040 control chromosomes in the GnomAD database, including 5,673 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as protective,risk factor (no stars).

Frequency

Genomes: 𝑓 0.25 ( 5673 hom., cov: 32)

Consequence

Unknown

Scores

2

Clinical Significance

protective; risk factor no assertion criteria provided B:1O:2

Conservation

PhyloP100: 0.0700
Variant links:

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ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

BP4
Computational evidence support a benign effect (BayesDel_noAF=-0.98).
BA1
GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.407 is higher than 0.05.

Transcripts

RefSeq

Gene Transcript HGVSc HGVSp Effect #exon/exons MANE Protein UniProt

Ensembl

Gene Transcript HGVSc HGVSp Effect #exon/exons TSL MANE Protein Appris UniProt

Frequencies

GnomAD3 genomes
AF:
0.253
AC:
38427
AN:
151922
Hom.:
5678
Cov.:
32
show subpopulations
Gnomad AFR
AF:
0.413
Gnomad AMI
AF:
0.406
Gnomad AMR
AF:
0.180
Gnomad ASJ
AF:
0.233
Gnomad EAS
AF:
0.0702
Gnomad SAS
AF:
0.192
Gnomad FIN
AF:
0.200
Gnomad MID
AF:
0.259
Gnomad NFE
AF:
0.198
Gnomad OTH
AF:
0.236
We have no GnomAD4 exomes data on this position. Probably position not covered by the project.
GnomAD4 genome
AF:
0.253
AC:
38427
AN:
152040
Hom.:
5673
Cov.:
32
AF XY:
0.250
AC XY:
18571
AN XY:
74336
show subpopulations
Gnomad4 AFR
AF:
0.412
Gnomad4 AMR
AF:
0.180
Gnomad4 ASJ
AF:
0.233
Gnomad4 EAS
AF:
0.0702
Gnomad4 SAS
AF:
0.191
Gnomad4 FIN
AF:
0.200
Gnomad4 NFE
AF:
0.198
Gnomad4 OTH
AF:
0.234
Alfa
AF:
0.213
Hom.:
3482
Bravo
AF:
0.258
Asia WGS
AF:
0.166
AC:
579
AN:
3478

ClinVar

Significance: protective; risk factor
Submissions summary: Benign:1Other:2
Revision: no assertion criteria provided
LINK: link

Submissions by phenotype

Dengue fever, protection against Benign:1
protective, no assertion criteria providedliterature onlyOMIMFeb 01, 2006- -
Mycobacterium tuberculosis, susceptibility to Other:1
risk factor, no assertion criteria providedliterature onlyOMIMFeb 01, 2006- -
Susceptibility to HIV infection Other:1
risk factor, no assertion criteria providedliterature onlyOMIMFeb 01, 2006- -

Computational scores

Source: dbNSFP v4.3

Name
Calibrated prediction
Score
Prediction
BayesDel_noAF
Benign
-0.98
CADD
Benign
2.9
DANN
Benign
0.74

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Below is the list of publications found by LitVar. It may be empty.

Other links and lift over

dbSNP: rs4804803; hg19: chr19-7812733; API