6-163417980-T-C

Variant names:

• chr6-163417980-T-C
• rs3763197
• NM_006775.3:c.142+2645T>C

Variant summary

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

The NM_006775.3(QKI):​c.142+2645T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.145 in 151,508 control chromosomes in the GnomAD database, including 2,181 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 0.15 (2181 hom., cov: 33)
• Consequence: QKI NM_006775.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.03
• Publications: 5 publications found

Genes affected

QKI (HGNC:21100): (QKI, KH domain containing RNA binding) The protein encoded by this gene is an RNA-binding protein that regulates pre-mRNA splicing, export of mRNAs from the nucleus, protein translation, and mRNA stability. The encoded protein is involved in myelinization and oligodendrocyte differentiation and may play a role in schizophrenia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.75).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.319 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_006775.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	QKI	NM_006775.3	MANE Select	c.142+2645T>C		intron	N/A	NP_006766.1	Q96PU8-1
	QKI	NM_001301085.2		c.142+2645T>C		intron	N/A	NP_001288014.1	Q96PU8-3
	QKI	NM_206854.3		c.142+2645T>C		intron	N/A	NP_996736.1	Q96PU8-6

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	QKI	ENST00000361752.8	TSL:1 MANE Select	c.142+2645T>C		intron	N/A	ENSP00000355094.3	Q96PU8-1
	QKI	ENST00000361195.6	TSL:1	c.142+2645T>C		intron	N/A	ENSP00000354867.2	Q96PU8-3
	QKI	ENST00000275262.11	TSL:1	c.142+2645T>C		intron	N/A	ENSP00000275262.7	Q96PU8-6

Frequencies

GnomAD3 genomes AF: 0.145 AC: 22024 AN: 151394 Hom.: 2177 Cov.: 33

Gnomad AFR AF: 0.0462

Gnomad AMI AF: 0.159

Gnomad AMR AF: 0.326

Gnomad ASJ AF: 0.186

Gnomad EAS AF: 0.259

Gnomad SAS AF: 0.134

Gnomad FIN AF: 0.132

Gnomad MID AF: 0.199

Gnomad NFE AF: 0.156

Gnomad OTH AF: 0.182

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

GnomAD4 genome AF: 0.145 AC: 22021 AN: 151508 Hom.: 2181 Cov.: 33 AF XY: 0.148 AC XY: 10962 AN XY: 74046

African (AFR) AF: 0.0461 AC: 1909 AN: 41374

American (AMR) AF: 0.326 AC: 4972 AN: 15248

Ashkenazi Jewish (ASJ) AF: 0.186 AC: 642 AN: 3458

East Asian (EAS) AF: 0.260 AC: 1341 AN: 5164

South Asian (SAS) AF: 0.134 AC: 641 AN: 4800

European-Finnish (FIN) AF: 0.132 AC: 1382 AN: 10436

Middle Eastern (MID) AF: 0.185 AC: 54 AN: 292

European-Non Finnish (NFE) AF: 0.156 AC: 10557 AN: 67724

Other (OTH) AF: 0.180 AC: 378 AN: 2102

Alfa AF: 0.139 Hom.: 852

Bravo AF: 0.158

Asia WGS AF: 0.162 AC: 561 AN: 3474

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.75
CADD	Benign	6.5
DANN	Benign	0.85
PhyloP100		-1.0
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: rs3763197; hg19: chr6-163839012;