rs4775854

Variant names:

• chr15-50121708-G-A
• rs4775854
• ENST00000558829.1:c.-42-14700C>T

Variant summary

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

The ENST00000558829.1(ATP8B4):​c.-42-14700C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.214 in 151,898 control chromosomes in the GnomAD database, including 3,967 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 0.21 (3967 hom., cov: 32)
• Consequence: ATP8B4 ENST00000558829.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.76
• Publications: 1 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=-0.95).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.272 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ATP8B4	XM_011522056.4	c.-42-14700C>T		intron_variant	Intron 1 of 28		XP_011520358.3
ATP8B4	XM_047433082.1	c.-43+1162C>T		intron_variant	Intron 2 of 29		XP_047289038.1
ATP8B4	XM_017022587.3	c.-42-14700C>T		intron_variant	Intron 1 of 27		XP_016878076.2
ATP8B4	XM_047433096.1	c.-42-14700C>T		intron_variant	Intron 1 of 24		XP_047289052.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ATP8B4	ENST00000558829.1	c.-42-14700C>T		intron_variant	Intron 1 of 3	3		ENSP00000453539.1

Frequencies

GnomAD3 genomes AF: 0.214 AC: 32512 AN: 151784 Hom.: 3965 Cov.: 32

Gnomad AFR AF: 0.0835

Gnomad AMI AF: 0.255

Gnomad AMR AF: 0.189

Gnomad ASJ AF: 0.282

Gnomad EAS AF: 0.278

Gnomad SAS AF: 0.280

Gnomad FIN AF: 0.281

Gnomad MID AF: 0.297

Gnomad NFE AF: 0.275

Gnomad OTH AF: 0.219

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

GnomAD4 genome AF: 0.214 AC: 32507 AN: 151898 Hom.: 3967 Cov.: 32 AF XY: 0.215 AC XY: 15931 AN XY: 74250

African (AFR) AF: 0.0833 AC: 3452 AN: 41464

American (AMR) AF: 0.189 AC: 2880 AN: 15234

Ashkenazi Jewish (ASJ) AF: 0.282 AC: 978 AN: 3468

East Asian (EAS) AF: 0.277 AC: 1432 AN: 5162

South Asian (SAS) AF: 0.281 AC: 1356 AN: 4822

European-Finnish (FIN) AF: 0.281 AC: 2963 AN: 10550

Middle Eastern (MID) AF: 0.306 AC: 90 AN: 294

European-Non Finnish (NFE) AF: 0.275 AC: 18660 AN: 67886

Other (OTH) AF: 0.220 AC: 463 AN: 2106

Alfa AF: 0.248 Hom.: 625

Bravo AF: 0.201

Asia WGS AF: 0.234 AC: 820 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.95
CADD	Benign	0.097
DANN	Benign	0.78
PhyloP100		-1.8

Splicing

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

Other links and lift over

dbSNP: rs4775854; hg19: chr15-50413905;