8-11187652-G-A

Variant names:

• chr8-11187652-G-A
• rs7819412
• NM_173683.4:c.764+12924C>T

Variant summary

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

The NM_173683.4(XKR6):​c.764+12924C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.575 in 152,006 control chromosomes in the GnomAD database, including 28,489 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 0.57 (28489 hom., cov: 31)
• Consequence: XKR6 NM_173683.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0460
• Publications: 69 publications found

Genes affected

XKR6 (HGNC:27806): (XK related 6) Predicted to be involved in apoptotic process involved in development; engulfment of apoptotic cell; and phosphatidylserine exposure on apoptotic cell surface. Predicted to be integral component of membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.868 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_173683.4. 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
	XKR6	NM_173683.4	MANE Select	c.764+12924C>T		intron	N/A	NP_775954.2
	XKR6	NR_138152.2		n.1389+7439C>T		intron	N/A
	XKR6	NR_138153.2		n.1258+12924C>T		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	XKR6	ENST00000416569.3	TSL:1 MANE Select	c.764+12924C>T		intron	N/A	ENSP00000416707.2
	XKR6	ENST00000529336.1	TSL:3	n.257+12924C>T		intron	N/A	ENSP00000436594.1

Frequencies

GnomAD3 genomes AF: 0.575 AC: 87265 AN: 151886 Hom.: 28436 Cov.: 31

Gnomad AFR AF: 0.875

Gnomad AMI AF: 0.394

Gnomad AMR AF: 0.402

Gnomad ASJ AF: 0.616

Gnomad EAS AF: 0.0686

Gnomad SAS AF: 0.435

Gnomad FIN AF: 0.371

Gnomad MID AF: 0.592

Gnomad NFE AF: 0.511

Gnomad OTH AF: 0.548

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

GnomAD4 genome AF: 0.575 AC: 87364 AN: 152006 Hom.: 28489 Cov.: 31 AF XY: 0.560 AC XY: 41616 AN XY: 74298

African (AFR) AF: 0.875 AC: 36305 AN: 41468

American (AMR) AF: 0.401 AC: 6129 AN: 15266

Ashkenazi Jewish (ASJ) AF: 0.616 AC: 2135 AN: 3468

East Asian (EAS) AF: 0.0686 AC: 354 AN: 5162

South Asian (SAS) AF: 0.435 AC: 2095 AN: 4812

European-Finnish (FIN) AF: 0.371 AC: 3918 AN: 10548

Middle Eastern (MID) AF: 0.592 AC: 174 AN: 294

European-Non Finnish (NFE) AF: 0.511 AC: 34755 AN: 67970

Other (OTH) AF: 0.541 AC: 1140 AN: 2106

Alfa AF: 0.522 Hom.: 83578

Bravo AF: 0.583

Asia WGS AF: 0.300 AC: 1046 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	1.1
DANN	Benign	0.24
PhyloP100		0.046
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: rs7819412; hg19: chr8-11045161;