rs4745805

chr10-76007736-T-C

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP4_Moderate BA1

The NM_001305581.2(LRMDA):c.132-28272T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.331 in 152,092 control chromosomes in the GnomAD database, including 9,710 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 0.33 (9710 hom., cov: 32)
• Consequence: LRMDA NM_001305581.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.98

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 -10 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.32).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.431 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
LRMDA	NM_001305581.2	c.132-28272T>C		intron_variant		ENST00000611255.5
LRMDA	NM_032024.5	c.48-28272T>C		intron_variant
LRMDA	NR_131178.2	n.486-28272T>C		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
LRMDA	ENST00000611255.5	c.132-28272T>C		intron_variant		5	NM_001305581.2	P1
LRMDA	ENST00000372499.5	c.48-28272T>C		intron_variant		1
LRMDA	ENST00000593699.5	n.486-28272T>C		intron_variant, non_coding_transcript_variant		1
LRMDA	ENST00000593817.1	n.93-28272T>C		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.331 AC: 50348 AN: 151976 Hom.: 9707 Cov.: 32

Gnomad AFR AF: 0.183

Gnomad AMI AF: 0.249

Gnomad AMR AF: 0.288

Gnomad ASJ AF: 0.473

Gnomad EAS AF: 0.0114

Gnomad SAS AF: 0.258

Gnomad FIN AF: 0.453

Gnomad MID AF: 0.373

Gnomad NFE AF: 0.435

Gnomad OTH AF: 0.361

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

GnomAD4 genome AF: 0.331 AC: 50347 AN: 152092 Hom.: 9710 Cov.: 32 AF XY: 0.329 AC XY: 24444 AN XY: 74346

Gnomad4 AFR AF: 0.182

Gnomad4 AMR AF: 0.287

Gnomad4 ASJ AF: 0.473

Gnomad4 EAS AF: 0.0112

Gnomad4 SAS AF: 0.258

Gnomad4 FIN AF: 0.453

Gnomad4 NFE AF: 0.435

Gnomad4 OTH AF: 0.357

Alfa AF: 0.385 Hom.: 1765

Bravo AF: 0.312

Asia WGS AF: 0.145 AC: 506 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.32
Cadd	Benign	18
Dann	Benign	0.66

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: rs4745805; hg19: chr10-77767494;