rs6792584

Variant names:

• chr3-67480964-G-A
• rs6792584
• NM_003848.4:c.1062+14834C>T

Your query was ambiguous. Multiple possible variants found:

• chr3-67480964-G-A
• chr3-67480964-G-T

Variant summary

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

The NM_003848.4(SUCLG2):​c.1062+14834C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.774 in 152,114 control chromosomes in the GnomAD database, including 45,909 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 0.77 (45909 hom., cov: 32)
• Consequence: SUCLG2 NM_003848.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.985
• Publications: 12 publications found

Genes affected

SUCLG2 (HGNC:11450): (succinate-CoA ligase GDP-forming subunit beta) This gene encodes a GTP-specific beta subunit of succinyl-CoA synthetase. Succinyl-CoA synthetase catalyzes the reversible reaction involving the formation of succinyl-CoA and succinate. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 5 and 12. [provided by RefSeq, Apr 2010]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.829 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SUCLG2	NM_003848.4	c.1062+14834C>T		intron_variant	Intron 9 of 10	ENST00000307227.10	NP_003839.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SUCLG2	ENST00000307227.10	c.1062+14834C>T		intron_variant	Intron 9 of 10	1	NM_003848.4	ENSP00000307432.5
SUCLG2	ENST00000493112.5	c.1062+14834C>T		intron_variant	Intron 9 of 10	1		ENSP00000419325.1
SUCLG2	ENST00000460567.5	c.333+37283C>T		intron_variant	Intron 3 of 4	1		ENSP00000417260.1
SUCLG2	ENST00000492795.1	c.1062+14834C>T		intron_variant	Intron 9 of 9	2		ENSP00000417589.1

Frequencies

GnomAD3 genomes AF: 0.774 AC: 117720 AN: 151996 Hom.: 45869 Cov.: 32

Gnomad AFR AF: 0.836

Gnomad AMI AF: 0.773

Gnomad AMR AF: 0.839

Gnomad ASJ AF: 0.784

Gnomad EAS AF: 0.797

Gnomad SAS AF: 0.752

Gnomad FIN AF: 0.612

Gnomad MID AF: 0.782

Gnomad NFE AF: 0.746

Gnomad OTH AF: 0.797

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

GnomAD4 genome AF: 0.774 AC: 117810 AN: 152114 Hom.: 45909 Cov.: 32 AF XY: 0.771 AC XY: 57282 AN XY: 74326

African (AFR) AF: 0.836 AC: 34727 AN: 41526

American (AMR) AF: 0.840 AC: 12836 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.784 AC: 2721 AN: 3470

East Asian (EAS) AF: 0.797 AC: 4115 AN: 5160

South Asian (SAS) AF: 0.752 AC: 3621 AN: 4814

European-Finnish (FIN) AF: 0.612 AC: 6449 AN: 10544

Middle Eastern (MID) AF: 0.793 AC: 233 AN: 294

European-Non Finnish (NFE) AF: 0.746 AC: 50735 AN: 67992

Other (OTH) AF: 0.790 AC: 1670 AN: 2114

Alfa AF: 0.760 Hom.: 204920

Bravo AF: 0.795

Asia WGS AF: 0.750 AC: 2608 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.11
DANN	Benign	0.45
PhyloP100		-0.98
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: rs6792584; hg19: chr3-67531388;