18-51263449-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 0.0656 in 152,186 control chromosomes in the GnomAD database, including 701 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 0.066 ( 701 hom., cov: 32)

Consequence

Unknown

Scores

2

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: -0.942
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=-0.89).
BA1
GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.169 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:
0.0655
AC:
9955
AN:
152068
Hom.:
694
Cov.:
32
show subpopulations
Gnomad AFR
AF:
0.172
Gnomad AMI
AF:
0.0363
Gnomad AMR
AF:
0.0345
Gnomad ASJ
AF:
0.0375
Gnomad EAS
AF:
0.110
Gnomad SAS
AF:
0.0405
Gnomad FIN
AF:
0.0245
Gnomad MID
AF:
0.0669
Gnomad NFE
AF:
0.0146
Gnomad OTH
AF:
0.0535
We have no GnomAD4 exomes data on this position. Probably position not covered by the project.
GnomAD4 genome
AF:
0.0656
AC:
9990
AN:
152186
Hom.:
701
Cov.:
32
AF XY:
0.0658
AC XY:
4897
AN XY:
74404
show subpopulations
Gnomad4 AFR
AF:
0.172
Gnomad4 AMR
AF:
0.0345
Gnomad4 ASJ
AF:
0.0375
Gnomad4 EAS
AF:
0.110
Gnomad4 SAS
AF:
0.0397
Gnomad4 FIN
AF:
0.0245
Gnomad4 NFE
AF:
0.0146
Gnomad4 OTH
AF:
0.0549
Alfa
AF:
0.0287
Hom.:
86
Bravo
AF:
0.0703
Asia WGS
AF:
0.0830
AC:
289
AN:
3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name
Calibrated prediction
Score
Prediction
BayesDel_noAF
Benign
-0.89
CADD
Benign
0.24
DANN
Benign
0.78

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: rs16953030; hg19: chr18-48789819; API