rs116117580

chr2-47512394-G-A

Variant summary

Our verdict is Benign. Variant got -9 ACMG points: 0P and 9B. BP4_Strong BS1_Supporting BS2

The ENST00000406134.5(MSH2):c.2726G>A(p.Arg909Gln) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0181 in 1,611,322 control chromosomes in the GnomAD database, including 349 homozygotes. In-silico tool predicts a benign outcome for this variant. 11/12 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as not provided (no stars). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. R909W) has been classified as Benign.

• Frequency:
  • Genomes: 𝑓 0.012 (15 hom., cov: 32)
  • Exomes 𝑓: 0.019 (334 hom.)
• Consequence: MSH2 ENST00000406134.5 missense
• Clinical Significance: not provided no classification provided O:1
• Conservation: PhyloP100: -1.53

Genes affected

MSH2 (HGNC:7325): (mutS homolog 2) This locus is frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). When cloned, it was discovered to be a human homolog of the E. coli mismatch repair gene mutS, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]

KCNK12 (HGNC:6274): (potassium two pore domain channel subfamily K member 12) This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel, however, it may require other non-pore-forming proteins for activity. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -9 ACMG points.

• BP4: Computational evidence support a benign effect (MetaRNN=0.003568858).
• BS1: Variant frequency is greater than expected in population nfe. gnomad4 allele frequency = 0.0118 (1799/152234) while in subpopulation NFE AF= 0.0188 (1276/67986). AF 95% confidence interval is 0.0179. There are 15 homozygotes in gnomad4. There are 788 alleles in male gnomad4 subpopulation. This position pass quality control queck. Existence of Clinvar submissions makes me limit the strength of this signal to Supporting
• BS2: High Homozygotes in GnomAd at 15 AD,AR gene

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
KCNK12	NM_022055.2	c.*8513C>T		3_prime_UTR_variant	2/2	ENST00000327876.5

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
KCNK12	ENST00000327876.5	c.*8513C>T		3_prime_UTR_variant	2/2	1	NM_022055.2	P1

Frequencies

GnomAD3 genomes AF: 0.0118 AC: 1799 AN: 152116 Hom.: 15 Cov.: 32

Gnomad AFR AF: 0.00365

Gnomad AMI AF: 0.00658

Gnomad AMR AF: 0.0101

Gnomad ASJ AF: 0.0294

Gnomad EAS AF: 0.000192

Gnomad SAS AF: 0.000207

Gnomad FIN AF: 0.00698

Gnomad MID AF: 0.0127

Gnomad NFE AF: 0.0188

Gnomad OTH AF: 0.0139

GnomAD3 exomes AF: 0.0116 AC: 2755 AN: 238202 Hom.: 35 AF XY: 0.0117 AC XY: 1535 AN XY: 130656

Gnomad AFR exome AF: 0.00356

Gnomad AMR exome AF: 0.00541

Gnomad ASJ exome AF: 0.0275

Gnomad EAS exome AF: 0.00

Gnomad SAS exome AF: 0.000572

Gnomad FIN exome AF: 0.00730

Gnomad NFE exome AF: 0.0189

Gnomad OTH exome AF: 0.0132

GnomAD4 exome AF: 0.0187 AC: 27336 AN: 1459088 Hom.: 334 Cov.: 30 AF XY: 0.0182 AC XY: 13196 AN XY: 725636

Gnomad4 AFR exome AF: 0.00269

Gnomad4 AMR exome AF: 0.00616

Gnomad4 ASJ exome AF: 0.0285

Gnomad4 EAS exome AF: 0.00

Gnomad4 SAS exome AF: 0.000909

Gnomad4 FIN exome AF: 0.00799

Gnomad4 NFE exome AF: 0.0223

Gnomad4 OTH exome AF: 0.0143

GnomAD4 genome AF: 0.0118 AC: 1799 AN: 152234 Hom.: 15 Cov.: 32 AF XY: 0.0106 AC XY: 788 AN XY: 74430

Gnomad4 AFR AF: 0.00364

Gnomad4 AMR AF: 0.0101

Gnomad4 ASJ AF: 0.0294

Gnomad4 EAS AF: 0.000193

Gnomad4 SAS AF: 0.000207

Gnomad4 FIN AF: 0.00698

Gnomad4 NFE AF: 0.0188

Gnomad4 OTH AF: 0.0137

Alfa AF: 0.0160 Hom.: 14

Bravo AF: 0.0118

TwinsUK AF: 0.0210 AC: 78

ALSPAC AF: 0.0213 AC: 82

ESP6500AA AF: 0.00228 AC: 4

ESP6500EA AF: 0.0188 AC: 75

ExAC AF: 0.0112 AC: 1302

Asia WGS AF: 0.000577 AC: 2 AN: 3478

ClinVar

Significance: not provided

Submissions summary: Other:1

Revision: no classification provided

Submissions by phenotype

not specified Other:1

not provided, no classification provided

reference population

ITMI

Sep 19, 2013

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_addAF	Benign	-0.54	T
BayesDel_noAF	Benign	-0.53
Cadd	Benign	0.020
Dann	Benign	0.40
Eigen	Benign	-2.1
Eigen_PC	Benign	-2.2
FATHMM_MKL	Benign	0.0012	N
LIST_S2	Benign	0.41	T;T
MetaRNN	Benign	0.0036	T;T
MetaSVM	Benign	-0.80	T
MutationTaster	Benign	1.0	N
Polyphen		0.0	.;B
Vest4		0.024
ClinPred		0.00070	T
GERP RS		-5.2

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs116117580; hg19: chr2-47739533; COSMIC: COSV100009874; COSMIC: COSV100009874;