rs10509361

chr10-75793428-A-G

Variant summary

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

The NM_001305581.2(LRMDA):c.132-242580A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.399 in 152,006 control chromosomes in the GnomAD database, including 13,775 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 0.40 (13775 hom., cov: 32)
• Consequence: LRMDA NM_001305581.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.16

Genes affected

LRMDA (HGNC:23405): (leucine rich melanocyte differentiation associated) This gene encodes a leucine-rich repeat protein. The encoded protein is thought to play a role in melanocyte differentiation. Mutations in this gene have been associated with autosomal recessive oculocutaneous albinism 7 (OCA7). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.77).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.505 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
LRMDA	NM_001305581.2	c.132-242580A>G		intron_variant		ENST00000611255.5
LRMDA	NM_032024.5	c.47+10406A>G		intron_variant
LRMDA	NR_131178.2	n.86-89228A>G		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
LRMDA	ENST00000611255.5	c.132-242580A>G		intron_variant		5	NM_001305581.2	P1
LRMDA	ENST00000372499.5	c.47+10406A>G		intron_variant		1
LRMDA	ENST00000593699.5	n.86-89228A>G		intron_variant, non_coding_transcript_variant		1
LRMDA	ENST00000593817.1	n.92+192097A>G		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.399 AC: 60605 AN: 151886 Hom.: 13765 Cov.: 32

Gnomad AFR AF: 0.178

Gnomad AMI AF: 0.581

Gnomad AMR AF: 0.410

Gnomad ASJ AF: 0.353

Gnomad EAS AF: 0.341

Gnomad SAS AF: 0.522

Gnomad FIN AF: 0.527

Gnomad MID AF: 0.325

Gnomad NFE AF: 0.507

Gnomad OTH AF: 0.391

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

GnomAD4 genome AF: 0.399 AC: 60635 AN: 152006 Hom.: 13775 Cov.: 32 AF XY: 0.402 AC XY: 29892 AN XY: 74302

Gnomad4 AFR AF: 0.178

Gnomad4 AMR AF: 0.411

Gnomad4 ASJ AF: 0.353

Gnomad4 EAS AF: 0.341

Gnomad4 SAS AF: 0.522

Gnomad4 FIN AF: 0.527

Gnomad4 NFE AF: 0.507

Gnomad4 OTH AF: 0.390

Alfa AF: 0.472 Hom.: 9702

Bravo AF: 0.378

Asia WGS AF: 0.411 AC: 1430 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.77
Cadd	Benign	16
Dann	Benign	0.70

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: rs10509361; hg19: chr10-77553186;