rs245128

Variant names:

• chr5-135545302-T-C
• rs245128
• ENST00000698884.1:n.496+58533T>C

Your query was ambiguous. Multiple possible variants found:

• chr5-135545302-T-C
• chr5-135545302-T-G

Variant summary

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

The ENST00000698884.1(ENSG00000250167):​n.496+58533T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.531 in 152,068 control chromosomes in the GnomAD database, including 24,746 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 0.53 (24746 hom., cov: 32)
• Consequence: ENSG00000250167 ENST00000698884.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.677
• Publications: 1 publications found

Genes affected

ENSG00000250167 (HGNC:):

SLC25A48 (HGNC:30451): (solute carrier family 25 member 48) Predicted to enable acyl carnitine transmembrane transporter activity. Predicted to be involved in acyl carnitine transport and amino acid transport. Predicted to be located in mitochondrial inner membrane. Predicted to be integral component of 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=-0.78).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.65 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000698884.1. 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
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000250167	ENST00000698884.1		n.496+58533T>C		intron	N/A
	SLC25A48	ENST00000698885.1		n.364+35546T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.531 AC: 80666 AN: 151950 Hom.: 24742 Cov.: 32

Gnomad AFR AF: 0.202

Gnomad AMI AF: 0.827

Gnomad AMR AF: 0.655

Gnomad ASJ AF: 0.644

Gnomad EAS AF: 0.641

Gnomad SAS AF: 0.490

Gnomad FIN AF: 0.734

Gnomad MID AF: 0.614

Gnomad NFE AF: 0.655

Gnomad OTH AF: 0.573

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

GnomAD4 genome AF: 0.531 AC: 80684 AN: 152068 Hom.: 24746 Cov.: 32 AF XY: 0.535 AC XY: 39791 AN XY: 74342

African (AFR) AF: 0.202 AC: 8362 AN: 41486

American (AMR) AF: 0.655 AC: 10011 AN: 15286

Ashkenazi Jewish (ASJ) AF: 0.644 AC: 2233 AN: 3470

East Asian (EAS) AF: 0.641 AC: 3291 AN: 5134

South Asian (SAS) AF: 0.494 AC: 2377 AN: 4814

European-Finnish (FIN) AF: 0.734 AC: 7770 AN: 10592

Middle Eastern (MID) AF: 0.599 AC: 176 AN: 294

European-Non Finnish (NFE) AF: 0.655 AC: 44501 AN: 67968

Other (OTH) AF: 0.572 AC: 1209 AN: 2112

Alfa AF: 0.592 Hom.: 43703

Bravo AF: 0.515

Asia WGS AF: 0.535 AC: 1861 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
CADD	Benign	6.5
DANN	Benign	0.70
PhyloP100		0.68

Splicing

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

Other links and lift over

dbSNP: rs245128; hg19: chr5-134880992;