rs1408262

Variant names:

• chr6-18407487-A-T
• rs1408262
• NM_182757.4:c.165+7788A>T

Variant summary

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

The NM_182757.4(RNF144B):​c.165+7788A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.624 in 152,038 control chromosomes in the GnomAD database, including 30,119 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 0.62 (30119 hom., cov: 32)
• Consequence: RNF144B NM_182757.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.71
• Publications: 1 publications found

Genes affected

RNF144B (HGNC:21578): (ring finger protein 144B) Enables ubiquitin-protein transferase activity. Involved in negative regulation of apoptotic process and ubiquitin-dependent protein catabolic process. Located in mitochondrial 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=-0.9).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.689 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_182757.4. 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
	RNF144B	NM_182757.4	MANE Select	c.165+7788A>T		intron	N/A	NP_877434.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RNF144B	ENST00000259939.4	TSL:1 MANE Select	c.165+7788A>T		intron	N/A	ENSP00000259939.4

Frequencies

GnomAD3 genomes AF: 0.624 AC: 94845 AN: 151920 Hom.: 30115 Cov.: 32

Gnomad AFR AF: 0.514

Gnomad AMI AF: 0.856

Gnomad AMR AF: 0.606

Gnomad ASJ AF: 0.659

Gnomad EAS AF: 0.676

Gnomad SAS AF: 0.588

Gnomad FIN AF: 0.584

Gnomad MID AF: 0.680

Gnomad NFE AF: 0.694

Gnomad OTH AF: 0.655

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

GnomAD4 genome AF: 0.624 AC: 94882 AN: 152038 Hom.: 30119 Cov.: 32 AF XY: 0.620 AC XY: 46083 AN XY: 74316

African (AFR) AF: 0.513 AC: 21267 AN: 41440

American (AMR) AF: 0.606 AC: 9272 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.659 AC: 2287 AN: 3472

East Asian (EAS) AF: 0.678 AC: 3509 AN: 5178

South Asian (SAS) AF: 0.590 AC: 2842 AN: 4818

European-Finnish (FIN) AF: 0.584 AC: 6150 AN: 10534

Middle Eastern (MID) AF: 0.684 AC: 201 AN: 294

European-Non Finnish (NFE) AF: 0.694 AC: 47188 AN: 67980

Other (OTH) AF: 0.655 AC: 1385 AN: 2114

Alfa AF: 0.646 Hom.: 3991

Bravo AF: 0.622

Asia WGS AF: 0.641 AC: 2227 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.23
DANN	Benign	0.65
PhyloP100		-1.7
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: rs1408262; hg19: chr6-18407718;