NM_000534.5:c.582+1876A>G

Variant names:

• chr2-189820056-A-G
• rs1233276
• NM_000534.5:c.582+1876A>G

Variant summary

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

The NM_000534.5(PMS1):​c.582+1876A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.234 in 152,160 control chromosomes in the GnomAD database, including 4,353 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 0.23 (4353 hom., cov: 32)
• Consequence: PMS1 NM_000534.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.187
• Publications: 15 publications found

Genes affected

PMS1 (HGNC:9121): (PMS1 homolog 1, mismatch repair system component) This gene encodes a protein belonging to the DNA mismatch repair mutL/hexB family. This protein is thought to be involved in the repair of DNA mismatches, and it can form heterodimers with MLH1, a known DNA mismatch repair protein. Mutations in this gene cause hereditary nonpolyposis colorectal cancer type 3 (HNPCC3) either alone or in combination with mutations in other genes involved in the HNPCC phenotype, which is also known as Lynch syndrome. [provided by RefSeq, Jul 2008]

PMS1 Gene-Disease associations (from GenCC):

• Lynch syndrome

  Inheritance: AD Classification: NO_KNOWN Submitted by: ClinGen

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.297 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_000534.5. 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
	PMS1	NM_000534.5	MANE Select	c.582+1876A>G		intron	N/A	NP_000525.1
	PMS1	NM_001321045.2		c.582+1876A>G		intron	N/A	NP_001307974.1
	PMS1	NM_001321047.2		c.582+1876A>G		intron	N/A	NP_001307976.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PMS1	ENST00000441310.7	TSL:1 MANE Select	c.582+1876A>G		intron	N/A	ENSP00000406490.3
	PMS1	ENST00000409593.5	TSL:1	c.54+1876A>G		intron	N/A	ENSP00000387169.1
	PMS1	ENST00000424059.1	TSL:1	n.582+1876A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.234 AC: 35508 AN: 152044 Hom.: 4345 Cov.: 32

Gnomad AFR AF: 0.301

Gnomad AMI AF: 0.133

Gnomad AMR AF: 0.188

Gnomad ASJ AF: 0.241

Gnomad EAS AF: 0.147

Gnomad SAS AF: 0.194

Gnomad FIN AF: 0.220

Gnomad MID AF: 0.291

Gnomad NFE AF: 0.215

Gnomad OTH AF: 0.239

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

GnomAD4 genome AF: 0.234 AC: 35533 AN: 152160 Hom.: 4353 Cov.: 32 AF XY: 0.233 AC XY: 17312 AN XY: 74384

African (AFR) AF: 0.302 AC: 12511 AN: 41490

American (AMR) AF: 0.188 AC: 2870 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.241 AC: 838 AN: 3470

East Asian (EAS) AF: 0.146 AC: 760 AN: 5188

South Asian (SAS) AF: 0.192 AC: 926 AN: 4826

European-Finnish (FIN) AF: 0.220 AC: 2330 AN: 10592

Middle Eastern (MID) AF: 0.271 AC: 79 AN: 292

European-Non Finnish (NFE) AF: 0.215 AC: 14591 AN: 67990

Other (OTH) AF: 0.240 AC: 507 AN: 2112

Alfa AF: 0.220 Hom.: 5314

Bravo AF: 0.231

Asia WGS AF: 0.204 AC: 709 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	3.3
DANN	Benign	0.54
PhyloP100		0.19
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: rs1233276; hg19: chr2-190684782;