rs3131379

chr6-31753256-G-A

Variant summary

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

The NM_172166.4(MSH5):c.813-45G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.102 in 1,558,426 control chromosomes in the GnomAD database, including 10,108 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 0.077 (559 hom., cov: 32)
  • Exomes 𝑓: 0.11 (9549 hom.)
• Consequence: MSH5 NM_172166.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.505

Genes affected

MSH5 (HGNC:7328): (mutS homolog 5) This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene. [provided by RefSeq, Feb 2011]

MSH5-SAPCD1 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.105 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MSH5	NM_172166.4	c.813-45G>A		intron_variant		ENST00000375750.9
MSH5-SAPCD1	NR_037846.1	n.992-45G>A		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MSH5	ENST00000375750.9	c.813-45G>A		intron_variant		1	NM_172166.4	A2

Frequencies

GnomAD3 genomes AF: 0.0767 AC: 11663 AN: 152126 Hom.: 559 Cov.: 32

Gnomad AFR AF: 0.0627

Gnomad AMI AF: 0.0691

Gnomad AMR AF: 0.0374

Gnomad ASJ AF: 0.0398

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00145

Gnomad FIN AF: 0.0792

Gnomad MID AF: 0.0222

Gnomad NFE AF: 0.108

Gnomad OTH AF: 0.0599

GnomAD3 exomes AF: 0.0645 AC: 14212 AN: 220496 Hom.: 730 AF XY: 0.0632 AC XY: 7478 AN XY: 118258

Gnomad AFR exome AF: 0.0614

Gnomad AMR exome AF: 0.0239

Gnomad ASJ exome AF: 0.0404

Gnomad EAS exome AF: 0.0000562

Gnomad SAS exome AF: 0.00175

Gnomad FIN exome AF: 0.0780

Gnomad NFE exome AF: 0.101

Gnomad OTH exome AF: 0.0642

GnomAD4 exome AF: 0.105 AC: 147653 AN: 1406182 Hom.: 9549 Cov.: 32 AF XY: 0.102 AC XY: 70344 AN XY: 691472

Gnomad4 AFR exome AF: 0.0645

Gnomad4 AMR exome AF: 0.0252

Gnomad4 ASJ exome AF: 0.0415

Gnomad4 EAS exome AF: 0.000103

Gnomad4 SAS exome AF: 0.00263

Gnomad4 FIN exome AF: 0.0808

Gnomad4 NFE exome AF: 0.124

Gnomad4 OTH exome AF: 0.0915

GnomAD4 genome AF: 0.0766 AC: 11664 AN: 152244 Hom.: 559 Cov.: 32 AF XY: 0.0712 AC XY: 5301 AN XY: 74434

Gnomad4 AFR AF: 0.0626

Gnomad4 AMR AF: 0.0372

Gnomad4 ASJ AF: 0.0398

Gnomad4 EAS AF: 0.00

Gnomad4 SAS AF: 0.00145

Gnomad4 FIN AF: 0.0792

Gnomad4 NFE AF: 0.108

Gnomad4 OTH AF: 0.0592

Alfa AF: 0.0931 Hom.: 1641

Bravo AF: 0.0733

Asia WGS AF: 0.00837 AC: 30 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
Cadd	Benign	3.5
Dann	Benign	0.67

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.020		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: rs3131379; hg19: chr6-31721033;