chr14-74286273-G-A

Variant names:

• chr14-74286273-G-A
• rs8618
• NM_005050.4:c.*188C>T

Variant summary

Our verdict is Benign. The variant received -20 ACMG points: 0P and 20B. BP4_Strong BP6_Very_Strong BA1

The NM_005050.4(ABCD4):​c.*188C>T variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0242 in 603,844 control chromosomes in the GnomAD database, including 1,664 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.070 (1284 hom., cov: 33)
  • Exomes 𝑓: 0.0088 (380 hom.)
• Consequence: ABCD4 NM_005050.4 3_prime_UTR
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:2
• Conservation: PhyloP100: 1.19

Genes affected

ABCD4 (HGNC:68): (ATP binding cassette subfamily D member 4) The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. The function of this peroxisomal membrane protein is unknown. However, it is speculated that it may function as a heterodimer for another peroxisomal ABC transporter and, therefore, may modify the adrenoleukodystrophy phenotype. It may also play a role in the process of peroxisome biogenesis. Alternative splicing results in several protein-coding and non-protein-coding variants. [provided by RefSeq, Jul 2017]

ACMG classification

Our verdict: Benign. The variant received -20 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).
• BP6: Variant 14-74286273-G-A is Benign according to our data. Variant chr14-74286273-G-A is described in ClinVar as [Benign]. Clinvar id is 1292532.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.239 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ABCD4	NM_005050.4	c.*188C>T		3_prime_UTR_variant	Exon 19 of 19	ENST00000356924.9	NP_005041.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ABCD4	ENST00000356924	c.*188C>T		3_prime_UTR_variant	Exon 19 of 19	1	NM_005050.4	ENSP00000349396.4

Frequencies

GnomAD3 genomes AF: 0.0698 AC: 10619 AN: 152162 Hom.: 1278 Cov.: 33

Gnomad AFR AF: 0.243

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.0258

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.000193

Gnomad SAS AF: 0.000620

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.0190

Gnomad NFE AF: 0.000794

Gnomad OTH AF: 0.0478

GnomAD4 exome AF: 0.00879 AC: 3969 AN: 451564 Hom.: 380 Cov.: 5 AF XY: 0.00736 AC XY: 1753 AN XY: 238158

Gnomad4 AFR exome AF: 0.243 AC: 3028 AN: 12436

Gnomad4 AMR exome AF: 0.0165 AC: 295 AN: 17898

Gnomad4 ASJ exome AF: 0.00 AC: 0 AN: 13246

Gnomad4 EAS exome AF: 0.00 AC: 0 AN: 30228

Gnomad4 SAS exome AF: 0.000441 AC: 20 AN: 45318

Gnomad4 FIN exome AF: 0.00 AC: 0 AN: 28562

Gnomad4 NFE exome AF: 0.000507 AC: 140 AN: 275970

Gnomad4 Remaining exome AF: 0.0183 AC: 466 AN: 25498

GnomAD4 genome AF: 0.0699 AC: 10647 AN: 152280 Hom.: 1284 Cov.: 33 AF XY: 0.0660 AC XY: 4911 AN XY: 74462

Gnomad4 AFR AF: 0.243 AC: 0.242932 AN: 0.242932

Gnomad4 AMR AF: 0.0258 AC: 0.0258102 AN: 0.0258102

Gnomad4 ASJ AF: 0.00 AC: 0 AN: 0

Gnomad4 EAS AF: 0.000194 AC: 0.000193648 AN: 0.000193648

Gnomad4 SAS AF: 0.000621 AC: 0.000620604 AN: 0.000620604

Gnomad4 FIN AF: 0.00 AC: 0 AN: 0

Gnomad4 NFE AF: 0.000794 AC: 0.000793697 AN: 0.000793697

Gnomad4 OTH AF: 0.0473 AC: 0.047259 AN: 0.047259

Alfa AF: 0.0522 Hom.: 226

Bravo AF: 0.0793

Asia WGS AF: 0.0170 AC: 60 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:2

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not provided Benign:2

-

Breakthrough Genomics, Breakthrough Genomics

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: not provided

- -

Feb 08, 2019

GeneDx

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
CADD	Benign	3.8
DANN	Benign	0.65
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

Publications

LitVar

Other links and lift over

dbSNP: rs8618; hg19: chr14-74752976;