chr4-1084399-G-A

Variant names:

• chr4-1084399-G-A
• rs1670533
• NM_001131034.4:c.362+1497C>T

Variant summary

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

The NM_001131034.4(RNF212):​c.362+1497C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.811 in 152,092 control chromosomes in the GnomAD database, including 50,705 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as association (no stars).

• Frequency: Genomes: 𝑓 0.81 (50705 hom., cov: 31)
• Consequence: RNF212 NM_001131034.4 intron
• Clinical Significance: association no assertion criteria provided O:1
• Conservation: PhyloP100: -1.31
• Publications: 43 publications found

Genes affected

RNF212 (HGNC:27729): (ring finger protein 212) This gene encodes a RING finger protein that may function as a ubiquitin ligase. The encoded protein may be involved in meiotic recombination. This gene is located within a linkage disequilibrium block and polymorphisms in this gene may influence recombination rates. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2010]

RNF212 Gene-Disease associations (from GenCC):

• spermatogenic failure 62

  Inheritance: AR Classification: LIMITED Submitted by: Labcorp Genetics (formerly Invitae)

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.03).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.932 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001131034.4. 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
	RNF212	NM_001131034.4	MANE Select	c.362+1497C>T		intron	N/A	NP_001124506.1	Q495C1-1
	RNF212	NM_001366919.1		c.362+1497C>T		intron	N/A	NP_001353848.1	A0A8V8TN20
	RNF212	NM_194439.5		c.362+1497C>T		intron	N/A	NP_919420.1	Q495C1-5

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RNF212	ENST00000433731.7	TSL:1 MANE Select	c.362+1497C>T		intron	N/A	ENSP00000389709.2	Q495C1-1
	RNF212	ENST00000382968.9	TSL:1	c.362+1497C>T		intron	N/A	ENSP00000372428.5	Q495C1-5
	RNF212	ENST00000698262.1		c.362+1497C>T		intron	N/A	ENSP00000513634.1	A0A8V8TN20

Frequencies

GnomAD3 genomes AF: 0.811 AC: 123234 AN: 151974 Hom.: 50669 Cov.: 31

Gnomad AFR AF: 0.940

Gnomad AMI AF: 0.628

Gnomad AMR AF: 0.685

Gnomad ASJ AF: 0.784

Gnomad EAS AF: 0.619

Gnomad SAS AF: 0.757

Gnomad FIN AF: 0.804

Gnomad MID AF: 0.801

Gnomad NFE AF: 0.785

Gnomad OTH AF: 0.794

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

GnomAD4 genome AF: 0.811 AC: 123322 AN: 152092 Hom.: 50705 Cov.: 31 AF XY: 0.806 AC XY: 59953 AN XY: 74356

African (AFR) AF: 0.940 AC: 39013 AN: 41500

American (AMR) AF: 0.683 AC: 10442 AN: 15278

Ashkenazi Jewish (ASJ) AF: 0.784 AC: 2719 AN: 3470

East Asian (EAS) AF: 0.618 AC: 3191 AN: 5162

South Asian (SAS) AF: 0.757 AC: 3655 AN: 4826

European-Finnish (FIN) AF: 0.804 AC: 8485 AN: 10550

Middle Eastern (MID) AF: 0.793 AC: 233 AN: 294

European-Non Finnish (NFE) AF: 0.785 AC: 53345 AN: 67998

Other (OTH) AF: 0.792 AC: 1669 AN: 2106

Alfa AF: 0.785 Hom.: 180324

Bravo AF: 0.806

Asia WGS AF: 0.667 AC: 2320 AN: 3478

ClinVar

ClinVar submissions

Significance: association

Revision: no assertion criteria provided

Pathogenic	VUS	Benign	Condition
-	-	-	RECOMBINATION RATE QUANTITATIVE TRAIT LOCUS 1 (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	1.0
DANN	Benign	0.54
PhyloP100		-1.3
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: rs1670533; hg19: chr4-1078187;