chr11-69296043-G-A

Variant names:

• chr11-69296043-G-A
• rs11539762
• NM_001293291.2:c.593G>A

Variant summary

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

The NM_001293291.2(MYEOV):​c.593G>A​(p.Arg198Gln) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.12 in 1,614,078 control chromosomes in the GnomAD database, including 13,260 homozygotes. In-silico tool predicts a benign outcome for this variant. 14/20 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.11 (1073 hom., cov: 33)
  • Exomes 𝑓: 0.12 (12187 hom.)
• Consequence: MYEOV NM_001293291.2 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.339
• Publications: 22 publications found

Genes affected

MYEOV (HGNC:7563): (myeloma overexpressed)

ACMG classification

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

• BP4: Computational evidence support a benign effect (MetaRNN=0.0055698156).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.252 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001293291.2. 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
	MYEOV	NM_001293291.2	MANE Select	c.593G>A	p.Arg198Gln	missense	Exon 3 of 3	NP_001280220.1
	MYEOV	NM_138768.4		c.593G>A	p.Arg198Gln	missense	Exon 3 of 3	NP_620123.2
	MYEOV	NM_001293294.2		c.419G>A	p.Arg140Gln	missense	Exon 2 of 2	NP_001280223.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MYEOV	ENST00000441339.3	TSL:2 MANE Select	c.593G>A	p.Arg198Gln	missense	Exon 3 of 3	ENSP00000412482.2
	MYEOV	ENST00000308946.3	TSL:1	c.593G>A	p.Arg198Gln	missense	Exon 3 of 3	ENSP00000308330.3
	MYEOV	ENST00000535653.1	TSL:1	n.1224G>A		non_coding_transcript_exon	Exon 2 of 2

Frequencies

GnomAD3 genomes AF: 0.112 AC: 17097 AN: 152098 Hom.: 1075 Cov.: 33

Gnomad AFR AF: 0.106

Gnomad AMI AF: 0.0680

Gnomad AMR AF: 0.0962

Gnomad ASJ AF: 0.137

Gnomad EAS AF: 0.198

Gnomad SAS AF: 0.264

Gnomad FIN AF: 0.0669

Gnomad MID AF: 0.187

Gnomad NFE AF: 0.109

Gnomad OTH AF: 0.119

GnomAD2 exomes AF: 0.130 AC: 32669 AN: 251362 AF XY: 0.138

Gnomad AFR exome AF: 0.104

Gnomad AMR exome AF: 0.0759

Gnomad ASJ exome AF: 0.142

Gnomad EAS exome AF: 0.196

Gnomad FIN exome AF: 0.0749

Gnomad NFE exome AF: 0.114

Gnomad OTH exome AF: 0.129

GnomAD4 exome AF: 0.121 AC: 176999 AN: 1461862 Hom.: 12187 Cov.: 34 AF XY: 0.125 AC XY: 91152 AN XY: 727228

African (AFR) AF: 0.0970 AC: 3249 AN: 33478

American (AMR) AF: 0.0772 AC: 3454 AN: 44718

Ashkenazi Jewish (ASJ) AF: 0.144 AC: 3754 AN: 26136

East Asian (EAS) AF: 0.194 AC: 7716 AN: 39698

South Asian (SAS) AF: 0.256 AC: 22057 AN: 86258

European-Finnish (FIN) AF: 0.0765 AC: 4084 AN: 53406

Middle Eastern (MID) AF: 0.154 AC: 890 AN: 5768

European-Non Finnish (NFE) AF: 0.111 AC: 123966 AN: 1112004

Other (OTH) AF: 0.130 AC: 7829 AN: 60396

GnomAD4 genome AF: 0.112 AC: 17106 AN: 152216 Hom.: 1073 Cov.: 33 AF XY: 0.114 AC XY: 8503 AN XY: 74394

African (AFR) AF: 0.106 AC: 4410 AN: 41538

American (AMR) AF: 0.0960 AC: 1469 AN: 15300

Ashkenazi Jewish (ASJ) AF: 0.137 AC: 477 AN: 3472

East Asian (EAS) AF: 0.199 AC: 1026 AN: 5162

South Asian (SAS) AF: 0.264 AC: 1268 AN: 4810

European-Finnish (FIN) AF: 0.0669 AC: 710 AN: 10618

Middle Eastern (MID) AF: 0.194 AC: 57 AN: 294

European-Non Finnish (NFE) AF: 0.109 AC: 7380 AN: 68000

Other (OTH) AF: 0.117 AC: 247 AN: 2110

Alfa AF: 0.116 Hom.: 2198

Bravo AF: 0.109

TwinsUK AF: 0.111 AC: 412

ALSPAC AF: 0.125 AC: 482

ESP6500AA AF: 0.0984 AC: 433

ESP6500EA AF: 0.108 AC: 925

ExAC AF: 0.134 AC: 16288

Asia WGS AF: 0.222 AC: 771 AN: 3478

EpiCase AF: 0.113

EpiControl AF: 0.113

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.13
BayesDel_addAF	Benign	-0.79	T
BayesDel_noAF	Benign	-0.77
CADD	Benign	0.95
DANN	Benign	0.97
DEOGEN2	Benign	0.0024	T
Eigen	Benign	-0.75
Eigen_PC	Benign	-0.91
FATHMM_MKL	Benign	0.024	N
LIST_S2	Benign	0.52	T
MetaRNN	Benign	0.0056	T
MetaSVM	Benign	-0.99	T
MutationAssessor	Benign	0.0	N
PhyloP100		-0.34
PrimateAI	Benign	0.21	T
PROVEAN	Benign	-2.0	N
REVEL	Benign	0.093
Polyphen		0.98	D
Vest4		0.019
MPC		0.33
ClinPred		0.012	T
GERP RS		1.4
Varity_R		0.22
gMVP		0.068
Mutation Taster		=100/0	polymorphism (auto)

Splicing

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

Other links and lift over

dbSNP: rs11539762; hg19: chr11-69063510; COSMIC: COSV58293488; COSMIC: COSV58293488;