ENST00000343811.10:c.1211-1100G>T

Variant names:

• chr20-37144941-C-A
• rs1780682
• ENST00000343811.10:c.1211-1100G>T

Variant summary

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

The ENST00000343811.10(MROH8):​c.1211-1100G>T 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: 33)
• Consequence: MROH8 ENST00000343811.10 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.13
• Publications: 6 publications found

Genes affected

MROH8 (HGNC:16125): (maestro heat like repeat family member 8) The protein encoded by this gene belongs to the maestro heat-like repeat family. The exact function of this gene is not known, however, in a genome-wide association study using hippocampal atrophy as a quantitative trait, this gene has been associated with Alzheimer's disease (PMID:19668339). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]

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=-0.91).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MROH8	NM_152503.8	c.1211-1100G>T		intron_variant	Intron 10 of 24		NP_689716.4
MROH8	NM_213631.3	c.1211-1100G>T		intron_variant	Intron 10 of 13		NP_998796.1
MROH8	NM_213632.3	c.1106-1100G>T		intron_variant	Intron 9 of 12		NP_998797.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MROH8	ENST00000343811.10	c.1211-1100G>T		intron_variant	Intron 10 of 24	1		ENSP00000513568.1
MROH8	ENST00000400440.7	c.1211-1100G>T		intron_variant	Intron 10 of 13	1		ENSP00000513569.1
MROH8	ENST00000422138.2	c.1106-1100G>T		intron_variant	Intron 9 of 22	3		ENSP00000400468.2
MROH8	ENST00000421643.2	c.1106-1100G>T		intron_variant	Intron 9 of 12	2		ENSP00000513570.1

Frequencies

GnomAD3 genomes Cov.: 33

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

GnomAD4 genome Cov.: 33

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.054
DANN	Benign	0.61
PhyloP100		-2.1

Splicing

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

Other links and lift over

dbSNP: rs1780682; hg19: chr20-35773344;