rs2067885

Variant names:

• chr15-49929748-A-G
• rs2067885
• NM_024837.4:c.1642+1371T>C

Variant summary

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

The NM_024837.4(ATP8B4):​c.1642+1371T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.224 in 151,996 control chromosomes in the GnomAD database, including 4,904 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 0.22 (4904 hom., cov: 32)
• Consequence: ATP8B4 NM_024837.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.417
• Publications: 2 publications found

Genes affected

ATP8B4 (HGNC:13536): (ATPase phospholipid transporting 8B4 (putative)) This gene encodes a member of the cation transport ATPase (P-type) family and type IV subfamily. The encoded protein is involved in phospholipid transport in the cell membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.31 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ATP8B4	NM_024837.4	c.1642+1371T>C		intron_variant	Intron 16 of 27	ENST00000284509.11	NP_079113.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ATP8B4	ENST00000284509.11	c.1642+1371T>C		intron_variant	Intron 16 of 27	5	NM_024837.4	ENSP00000284509.6

Frequencies

GnomAD3 genomes AF: 0.224 AC: 34055 AN: 151878 Hom.: 4910 Cov.: 32

Gnomad AFR AF: 0.0725

Gnomad AMI AF: 0.309

Gnomad AMR AF: 0.201

Gnomad ASJ AF: 0.304

Gnomad EAS AF: 0.00329

Gnomad SAS AF: 0.167

Gnomad FIN AF: 0.373

Gnomad MID AF: 0.301

Gnomad NFE AF: 0.314

Gnomad OTH AF: 0.238

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

GnomAD4 genome AF: 0.224 AC: 34038 AN: 151996 Hom.: 4904 Cov.: 32 AF XY: 0.224 AC XY: 16657 AN XY: 74306

African (AFR) AF: 0.0722 AC: 3001 AN: 41540

American (AMR) AF: 0.201 AC: 3058 AN: 15250

Ashkenazi Jewish (ASJ) AF: 0.304 AC: 1052 AN: 3466

East Asian (EAS) AF: 0.00349 AC: 18 AN: 5160

South Asian (SAS) AF: 0.168 AC: 809 AN: 4808

European-Finnish (FIN) AF: 0.373 AC: 3934 AN: 10552

Middle Eastern (MID) AF: 0.293 AC: 86 AN: 294

European-Non Finnish (NFE) AF: 0.314 AC: 21303 AN: 67908

Other (OTH) AF: 0.235 AC: 495 AN: 2106

Alfa AF: 0.293 Hom.: 5733

Bravo AF: 0.208

Asia WGS AF: 0.0700 AC: 248 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	7.5
DANN	Benign	0.74
PhyloP100		0.42
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: rs2067885; hg19: chr15-50221945;