rs1585110

Variant names:

• chr4-153739792-C-T
• rs1585110
• NM_173662.4:c.246+8853G>A

Variant summary

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

The NM_173662.4(RNF175):​c.246+8853G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0593 in 152,092 control chromosomes in the GnomAD database, including 348 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 0.059 (348 hom., cov: 33)
• Consequence: RNF175 NM_173662.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.321
• Publications: 5 publications found

Genes affected

RNF175 (HGNC:27735): (ring finger protein 175) Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in ubiquitin-dependent ERAD pathway. Predicted to be integral component of membrane. Predicted to be active in Golgi membrane and endoplasmic reticulum 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=-1.01).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.0896 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_173662.4. 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
	RNF175	NM_173662.4	MANE Select	c.246+8853G>A		intron	N/A	NP_775933.2	Q8N4F7-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RNF175	ENST00000347063.9	TSL:1 MANE Select	c.246+8853G>A		intron	N/A	ENSP00000340979.4	Q8N4F7-1
	RNF175	ENST00000955649.1		c.305+5877G>A		intron	N/A	ENSP00000625708.1
	RNF175	ENST00000897861.1		c.246+8853G>A		intron	N/A	ENSP00000567920.1

Frequencies

GnomAD3 genomes AF: 0.0593 AC: 9017 AN: 151974 Hom.: 348 Cov.: 33

Gnomad AFR AF: 0.0139

Gnomad AMI AF: 0.146

Gnomad AMR AF: 0.0426

Gnomad ASJ AF: 0.0516

Gnomad EAS AF: 0.000385

Gnomad SAS AF: 0.0398

Gnomad FIN AF: 0.0908

Gnomad MID AF: 0.0190

Gnomad NFE AF: 0.0915

Gnomad OTH AF: 0.0489

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

GnomAD4 genome AF: 0.0593 AC: 9017 AN: 152092 Hom.: 348 Cov.: 33 AF XY: 0.0573 AC XY: 4264 AN XY: 74356

African (AFR) AF: 0.0139 AC: 575 AN: 41498

American (AMR) AF: 0.0424 AC: 648 AN: 15272

Ashkenazi Jewish (ASJ) AF: 0.0516 AC: 179 AN: 3472

East Asian (EAS) AF: 0.000386 AC: 2 AN: 5188

South Asian (SAS) AF: 0.0404 AC: 195 AN: 4824

European-Finnish (FIN) AF: 0.0908 AC: 956 AN: 10528

Middle Eastern (MID) AF: 0.0204 AC: 6 AN: 294

European-Non Finnish (NFE) AF: 0.0915 AC: 6222 AN: 67996

Other (OTH) AF: 0.0479 AC: 101 AN: 2110

Alfa AF: 0.0803 Hom.: 76

Bravo AF: 0.0535

Asia WGS AF: 0.0120 AC: 42 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	1.6
DANN	Benign	0.49
PhyloP100		-0.32
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: rs1585110; hg19: chr4-154660944;