rs6701572

chr1-51253643-G-A

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_014372.5(RNF11):c.124-16313G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.155 in 151,972 control chromosomes in the GnomAD database, including 2,825 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 0.16 (2825 hom., cov: 32)
• Consequence: RNF11 NM_014372.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.539

Genes affected

RNF11 (HGNC:10056): (ring finger protein 11) The protein encoded by this gene contains a RING-H2 finger motif, which is known to be important for protein-protein interactions. The expression of this gene has been shown to be induced by mutant RET proteins (MEN2A/MEN2B). The germline mutations in RET gene are known to be responsible for the development of multiple endocrine neoplasia (MEN). [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.01).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.331 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
RNF11	NM_014372.5	c.124-16313G>A		intron_variant		ENST00000242719.4

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
RNF11	ENST00000242719.4	c.124-16313G>A		intron_variant		1	NM_014372.5	P1
RNF11	ENST00000494873.1	n.541+16764G>A		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.155 AC: 23500 AN: 151856 Hom.: 2794 Cov.: 32

Gnomad AFR AF: 0.335

Gnomad AMI AF: 0.135

Gnomad AMR AF: 0.0885

Gnomad ASJ AF: 0.141

Gnomad EAS AF: 0.0993

Gnomad SAS AF: 0.0798

Gnomad FIN AF: 0.0562

Gnomad MID AF: 0.0854

Gnomad NFE AF: 0.0874

Gnomad OTH AF: 0.126

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

GnomAD4 genome AF: 0.155 AC: 23578 AN: 151972 Hom.: 2825 Cov.: 32 AF XY: 0.151 AC XY: 11257 AN XY: 74306

Gnomad4 AFR AF: 0.336

Gnomad4 AMR AF: 0.0883

Gnomad4 ASJ AF: 0.141

Gnomad4 EAS AF: 0.0993

Gnomad4 SAS AF: 0.0792

Gnomad4 FIN AF: 0.0562

Gnomad4 NFE AF: 0.0874

Gnomad4 OTH AF: 0.130

Alfa AF: 0.105 Hom.: 713

Bravo AF: 0.166

Asia WGS AF: 0.153 AC: 532 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
Cadd	Benign	2.8
Dann	Benign	0.65

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: rs6701572; hg19: chr1-51719315;