rs3766263

Variant names:

• chr1-67728828-C-T
• rs3766263
• NM_018841.6:c.-26-21116G>A

Variant summary

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

The NM_018841.6(GNG12):​c.-26-21116G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.476 in 151,962 control chromosomes in the GnomAD database, including 17,738 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 0.48 (17738 hom., cov: 32)
• Consequence: GNG12 NM_018841.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.236
• Publications: 1 publications found

Genes affected

GNG12 (HGNC:19663): (G protein subunit gamma 12) Enables PDZ domain binding activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.0).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.547 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
GNG12	NM_018841.6	c.-26-21116G>A		intron_variant	Intron 2 of 3	ENST00000370982.4	NP_061329.3
GNG12	XM_017001809.3	c.-26-21116G>A		intron_variant	Intron 2 of 3		XP_016857298.1
GNG12	XM_047425406.1	c.-27+11948G>A		intron_variant	Intron 3 of 4		XP_047281362.1
GNG12	XM_047425415.1	c.-26-21116G>A		intron_variant	Intron 3 of 4		XP_047281371.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
GNG12	ENST00000370982.4	c.-26-21116G>A		intron_variant	Intron 2 of 3	1	NM_018841.6	ENSP00000360021.3

Frequencies

GnomAD3 genomes AF: 0.476 AC: 72269 AN: 151844 Hom.: 17726 Cov.: 32

Gnomad AFR AF: 0.333

Gnomad AMI AF: 0.702

Gnomad AMR AF: 0.532

Gnomad ASJ AF: 0.505

Gnomad EAS AF: 0.428

Gnomad SAS AF: 0.564

Gnomad FIN AF: 0.503

Gnomad MID AF: 0.468

Gnomad NFE AF: 0.539

Gnomad OTH AF: 0.496

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

GnomAD4 genome AF: 0.476 AC: 72301 AN: 151962 Hom.: 17738 Cov.: 32 AF XY: 0.474 AC XY: 35215 AN XY: 74262

African (AFR) AF: 0.332 AC: 13762 AN: 41420

American (AMR) AF: 0.533 AC: 8133 AN: 15272

Ashkenazi Jewish (ASJ) AF: 0.505 AC: 1751 AN: 3468

East Asian (EAS) AF: 0.427 AC: 2206 AN: 5164

South Asian (SAS) AF: 0.565 AC: 2718 AN: 4812

European-Finnish (FIN) AF: 0.503 AC: 5305 AN: 10556

Middle Eastern (MID) AF: 0.469 AC: 137 AN: 292

European-Non Finnish (NFE) AF: 0.539 AC: 36600 AN: 67958

Other (OTH) AF: 0.498 AC: 1053 AN: 2114

Alfa AF: 0.517 Hom.: 4469

Bravo AF: 0.471

Asia WGS AF: 0.497 AC: 1730 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	3.1
DANN	Benign	0.52
PhyloP100		0.24
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: rs3766263; hg19: chr1-68194511;