NM_001198950.3:c.293-17350T>C

Variant names:

• chr13-108695311-T-C
• rs7984522
• NM_001198950.3:c.293-17350T>C

Variant summary

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

The NM_001198950.3(MYO16):​c.293-17350T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.231 in 152,082 control chromosomes in the GnomAD database, including 4,619 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 (4619 hom., cov: 32)
• Consequence: MYO16 NM_001198950.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.340
• Publications: 10 publications found

Genes affected

MYO16 (HGNC:29822): (myosin XVI) This gene encodes an unconventional myosin protein. The encoded protein has been proposed to act as a serine/threonine phosphatase-1 targeting or regulatory subunit. Studies in a rat cell line suggest that this protein may regulate cell cycle progression. A variant within this gene may be associated with susceptibility to schizophrenia and elevated expression of this gene has been observed in the frontal cortex of human schizophrenia patients. [provided by RefSeq, Mar 2017]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.436 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001198950.3. 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
	MYO16	NM_001198950.3	MANE Select	c.293-17350T>C		intron	N/A	NP_001185879.1
	MYO16	NM_015011.3		c.227-17350T>C		intron	N/A	NP_055826.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MYO16	ENST00000457511.7	TSL:1 MANE Select	c.293-17350T>C		intron	N/A	ENSP00000401633.3
	MYO16	ENST00000356711.7	TSL:1	c.227-17350T>C		intron	N/A	ENSP00000349145.2
	MYO16	ENST00000251041.10	TSL:5	c.227-17350T>C		intron	N/A	ENSP00000251041.5

Frequencies

GnomAD3 genomes AF: 0.230 AC: 34988 AN: 151964 Hom.: 4592 Cov.: 32

Gnomad AFR AF: 0.260

Gnomad AMI AF: 0.260

Gnomad AMR AF: 0.372

Gnomad ASJ AF: 0.155

Gnomad EAS AF: 0.451

Gnomad SAS AF: 0.252

Gnomad FIN AF: 0.266

Gnomad MID AF: 0.245

Gnomad NFE AF: 0.160

Gnomad OTH AF: 0.221

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

GnomAD4 genome AF: 0.231 AC: 35059 AN: 152082 Hom.: 4619 Cov.: 32 AF XY: 0.238 AC XY: 17712 AN XY: 74352

African (AFR) AF: 0.260 AC: 10785 AN: 41492

American (AMR) AF: 0.374 AC: 5705 AN: 15274

Ashkenazi Jewish (ASJ) AF: 0.155 AC: 539 AN: 3472

East Asian (EAS) AF: 0.451 AC: 2325 AN: 5150

South Asian (SAS) AF: 0.252 AC: 1212 AN: 4818

European-Finnish (FIN) AF: 0.266 AC: 2815 AN: 10586

Middle Eastern (MID) AF: 0.257 AC: 75 AN: 292

European-Non Finnish (NFE) AF: 0.160 AC: 10887 AN: 67976

Other (OTH) AF: 0.227 AC: 479 AN: 2110

Alfa AF: 0.182 Hom.: 11677

Bravo AF: 0.242

Asia WGS AF: 0.359 AC: 1247 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	3.7
DANN	Benign	0.82
PhyloP100		-0.34
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: rs7984522; hg19: chr13-109347659;