rs5982533

Variant names:

• chrX-112403236-C-G
• rs5982533
• NM_001395362.2:c.-284-27878C>G

Your query was ambiguous. Multiple possible variants found:

• chrX-112403236-C-G
• chrX-112403236-C-T

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001395362.2(RTL4):​c.-284-27878C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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: not found (cov: 22)
• Consequence: RTL4 NM_001395362.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.343
• Publications: 5 publications found

Genes affected

RTL4 (HGNC:25214): (retrotransposon Gag like 4) Predicted to enable nucleic acid binding activity and zinc ion binding activity. Predicted to act upstream of or within cognition and norepinephrine metabolic process. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RTL4	NM_001395362.2	c.-284-27878C>G		intron_variant	Intron 3 of 4	ENST00000695839.1	NP_001382291.1
RTL4	NM_001004308.3	c.-229-51264C>G		intron_variant	Intron 2 of 2		NP_001004308.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
RTL4	ENST00000695839.1	c.-284-27878C>G		intron_variant	Intron 3 of 4		NM_001395362.2	ENSP00000512211.1
RTL4	ENST00000340433.4	c.-284-27878C>G		intron_variant	Intron 2 of 3	6		ENSP00000340590.2
RTL4	ENST00000695808.1	c.-229-51264C>G		intron_variant	Intron 2 of 2			ENSP00000512188.1

Frequencies

GnomAD3 genomes Cov.: 22

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

GnomAD4 genome Cov.: 22

Alfa AF: 0.00 Hom.: 71423

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	3.2
DANN	Benign	0.68
PhyloP100		-0.34

Splicing

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

Other links and lift over

dbSNP: rs5982533; hg19: chrX-111646464;