chr2-210298339-T-TACACACACAC

Position:

• chr2-210298339-T-TACACACACAC

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP6_Moderate BA1

The NM_079420.3(MYL1):​c.304+80_304+81insGTGTGTGTGT variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0278 in 1,185,258 control chromosomes in the GnomAD database, including 209 homozygotes. Variant has been reported in ClinVar as Benign (★).

• Frequency:
  • Genomes: 𝑓 0.030 (101 hom., cov: 0)
  • Exomes 𝑓: 0.027 (108 hom.)
• Consequence: MYL1 NM_079420.3 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -1.73

Genes affected

MYL1 (HGNC:7582): (myosin light chain 1) Myosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatable alkali light chains, and two phosphorylatable regulatory light chains. This gene encodes a myosin alkali light chain expressed in fast skeletal muscle. Two transcript variants have been identified for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -10 ACMG points.

• BP6: Variant 2-210298339-T-TACACACACAC is Benign according to our data. Variant chr2-210298339-T-TACACACACAC is described in ClinVar as [Benign]. Clinvar id is 1270944.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.0543 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MYL1	NM_079420.3	c.304+80_304+81insGTGTGTGTGT		intron_variant		ENST00000352451.4
MYL1	NM_079422.3	c.172+80_172+81insGTGTGTGTGT		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MYL1	ENST00000352451.4	c.304+80_304+81insGTGTGTGTGT		intron_variant		1	NM_079420.3
MYL1	ENST00000341685.8	c.172+80_172+81insGTGTGTGTGT		intron_variant		1		P1
MYL1	ENST00000484290.1	n.435+80_435+81insGTGTGTGTGT		intron_variant, non_coding_transcript_variant		5
MYL1	ENST00000496436.5	n.407+80_407+81insGTGTGTGTGT		intron_variant, non_coding_transcript_variant		5

Frequencies

GnomAD3 genomes AF: 0.0304 AC: 4474 AN: 147258 Hom.: 101 Cov.: 0

Gnomad AFR AF: 0.0101

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.0542

Gnomad ASJ AF: 0.0443

Gnomad EAS AF: 0.0466

Gnomad SAS AF: 0.0602

Gnomad FIN AF: 0.0516

Gnomad MID AF: 0.0226

Gnomad NFE AF: 0.0308

Gnomad OTH AF: 0.0247

GnomAD4 exome AF: 0.0275 AC: 28498 AN: 1037892 Hom.: 108 AF XY: 0.0282 AC XY: 14941 AN XY: 528994

Gnomad4 AFR exome AF: 0.00758

Gnomad4 AMR exome AF: 0.0427

Gnomad4 ASJ exome AF: 0.0354

Gnomad4 EAS exome AF: 0.0463

Gnomad4 SAS exome AF: 0.0471

Gnomad4 FIN exome AF: 0.0432

Gnomad4 NFE exome AF: 0.0235

Gnomad4 OTH exome AF: 0.0258

GnomAD4 genome AF: 0.0304 AC: 4479 AN: 147366 Hom.: 101 Cov.: 0 AF XY: 0.0328 AC XY: 2345 AN XY: 71594

Gnomad4 AFR AF: 0.0100

Gnomad4 AMR AF: 0.0543

Gnomad4 ASJ AF: 0.0443

Gnomad4 EAS AF: 0.0471

Gnomad4 SAS AF: 0.0602

Gnomad4 FIN AF: 0.0516

Gnomad4 NFE AF: 0.0308

Gnomad4 OTH AF: 0.0249

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

May 21, 2021

- -

Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs112894708; hg19: chr2-211163063;