rs1182179

Variant names:

• chr7-2834014-A-G
• rs1182179
• NM_007353.3:c.309+9839T>C

Variant summary

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

The NM_007353.3(GNA12):​c.309+9839T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.249 in 152,144 control chromosomes in the GnomAD database, including 5,284 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 0.25 (5284 hom., cov: 32)
• Consequence: GNA12 NM_007353.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.97
• Publications: 18 publications found

Genes affected

GNA12 (HGNC:4380): (G protein subunit alpha 12) Predicted to enable D5 dopamine receptor binding activity; G-protein beta/gamma-subunit complex binding activity; and GTPase activity. Involved in regulation of TOR signaling and regulation of proteasomal ubiquitin-dependent protein catabolic process. Located in focal adhesion. [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=-1.01).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.293 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_007353.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GNA12	NM_007353.3	MANE Select	c.309+9839T>C		intron	N/A	NP_031379.2
	GNA12	NM_001293092.2		c.309+9839T>C		intron	N/A	NP_001280021.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GNA12	ENST00000275364.8	TSL:1 MANE Select	c.309+9839T>C		intron	N/A	ENSP00000275364.3
	GNA12	ENST00000715274.1		n.309+9839T>C		intron	N/A	ENSP00000520443.1
	GNA12	ENST00000715275.1		n.60+36610T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.249 AC: 37899 AN: 152028 Hom.: 5282 Cov.: 32

Gnomad AFR AF: 0.139

Gnomad AMI AF: 0.359

Gnomad AMR AF: 0.281

Gnomad ASJ AF: 0.262

Gnomad EAS AF: 0.199

Gnomad SAS AF: 0.158

Gnomad FIN AF: 0.384

Gnomad MID AF: 0.187

Gnomad NFE AF: 0.297

Gnomad OTH AF: 0.250

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

GnomAD4 genome AF: 0.249 AC: 37914 AN: 152144 Hom.: 5284 Cov.: 32 AF XY: 0.252 AC XY: 18711 AN XY: 74368

African (AFR) AF: 0.139 AC: 5785 AN: 41524

American (AMR) AF: 0.281 AC: 4289 AN: 15288

Ashkenazi Jewish (ASJ) AF: 0.262 AC: 910 AN: 3468

East Asian (EAS) AF: 0.199 AC: 1029 AN: 5172

South Asian (SAS) AF: 0.158 AC: 762 AN: 4818

European-Finnish (FIN) AF: 0.384 AC: 4061 AN: 10572

Middle Eastern (MID) AF: 0.184 AC: 54 AN: 294

European-Non Finnish (NFE) AF: 0.297 AC: 20166 AN: 67984

Other (OTH) AF: 0.251 AC: 531 AN: 2112

Alfa AF: 0.274 Hom.: 11475

Bravo AF: 0.238

Asia WGS AF: 0.229 AC: 797 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.040
DANN	Benign	0.52
PhyloP100		-2.0
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: rs1182179; hg19: chr7-2873648;