rs1330582

Positions:

• chr10-26263185-C-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001134366.2(GAD2):​c.921-5934C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.205 in 152,054 control chromosomes in the GnomAD database, including 3,370 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 0.20 (3370 hom., cov: 32)
• Consequence: GAD2 NM_001134366.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.120

Genes affected

GAD2 (HGNC:4093): (glutamate decarboxylase 2) This gene encodes one of several forms of glutamic acid decarboxylase, identified as a major autoantigen in insulin-dependent diabetes. The enzyme encoded is responsible for catalyzing the production of gamma-aminobutyric acid from L-glutamic acid. A pathogenic role for this enzyme has been identified in the human pancreas since it has been identified as an autoantibody and an autoreactive T cell target in insulin-dependent diabetes. This gene may also play a role in the stiff man syndrome. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Oct 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.293 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
GAD2	NM_001134366.2	c.921-5934C>T		intron_variant		ENST00000376261.8	NP_001127838.1
GAD2	NM_000818.3	c.921-5934C>T		intron_variant			NP_000809.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
GAD2	ENST00000376261.8	c.921-5934C>T		intron_variant		1	NM_001134366.2	ENSP00000365437.3
GAD2	ENST00000259271.7	c.921-5934C>T		intron_variant		1		ENSP00000259271.3
GAD2	ENST00000648567.1	c.579-5934C>T		intron_variant				ENSP00000498009.1

Frequencies

GnomAD3 genomes AF: 0.205 AC: 31110 AN: 151938 Hom.: 3365 Cov.: 32

Gnomad AFR AF: 0.247

Gnomad AMI AF: 0.246

Gnomad AMR AF: 0.198

Gnomad ASJ AF: 0.173

Gnomad EAS AF: 0.306

Gnomad SAS AF: 0.256

Gnomad FIN AF: 0.141

Gnomad MID AF: 0.288

Gnomad NFE AF: 0.180

Gnomad OTH AF: 0.212

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

GnomAD4 genome AF: 0.205 AC: 31126 AN: 152054 Hom.: 3370 Cov.: 32 AF XY: 0.206 AC XY: 15312 AN XY: 74338

Gnomad4 AFR AF: 0.247

Gnomad4 AMR AF: 0.198

Gnomad4 ASJ AF: 0.173

Gnomad4 EAS AF: 0.306

Gnomad4 SAS AF: 0.255

Gnomad4 FIN AF: 0.141

Gnomad4 NFE AF: 0.180

Gnomad4 OTH AF: 0.213

Alfa AF: 0.185 Hom.: 322

Bravo AF: 0.209

Asia WGS AF: 0.261 AC: 907 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.5
DANN	Benign	0.24

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

LitVar

Other links and lift over

dbSNP: rs1330582; hg19: chr10-26552114;