6-69735742-T-G

Position:

• chr6-69735742-T-G

Variant summary

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

The NM_018368.4(LMBRD1):​c.636+2200A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.364 in 152,064 control chromosomes in the GnomAD database, including 10,624 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 0.36 (10624 hom., cov: 32)
• Consequence: LMBRD1 NM_018368.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.487

Genes affected

LMBRD1 (HGNC:23038): (LMBR1 domain containing 1) This gene encodes a lysosomal membrane protein that may be involved in the transport and metabolism of cobalamin. This protein also interacts with the large form of the hepatitis delta antigen and may be required for the nucleocytoplasmic shuttling of the hepatitis delta virus. Mutations in this gene are associated with the vitamin B12 metabolism disorder termed, homocystinuria-megaloblastic anemia complementation type F.[provided by RefSeq, Oct 2009]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.79).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.527 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
LMBRD1	NM_018368.4	c.636+2200A>C		intron_variant		ENST00000649934.3	NP_060838.3
LMBRD1	NM_001363722.2	c.417+2200A>C		intron_variant			NP_001350651.1
LMBRD1	NM_001367271.1	c.417+2200A>C		intron_variant			NP_001354200.1
LMBRD1	NM_001367272.1	c.417+2200A>C		intron_variant			NP_001354201.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
LMBRD1	ENST00000649934.3	c.636+2200A>C		intron_variant			NM_018368.4	ENSP00000497690	P2

Frequencies

GnomAD3 genomes AF: 0.364 AC: 55354 AN: 151946 Hom.: 10617 Cov.: 32

Gnomad AFR AF: 0.249

Gnomad AMI AF: 0.400

Gnomad AMR AF: 0.392

Gnomad ASJ AF: 0.443

Gnomad EAS AF: 0.543

Gnomad SAS AF: 0.444

Gnomad FIN AF: 0.340

Gnomad MID AF: 0.475

Gnomad NFE AF: 0.407

Gnomad OTH AF: 0.386

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

GnomAD4 genome AF: 0.364 AC: 55381 AN: 152064 Hom.: 10624 Cov.: 32 AF XY: 0.363 AC XY: 26999 AN XY: 74346

Gnomad4 AFR AF: 0.249

Gnomad4 AMR AF: 0.393

Gnomad4 ASJ AF: 0.443

Gnomad4 EAS AF: 0.543

Gnomad4 SAS AF: 0.445

Gnomad4 FIN AF: 0.340

Gnomad4 NFE AF: 0.407

Gnomad4 OTH AF: 0.389

Alfa AF: 0.288 Hom.: 1033

Bravo AF: 0.361

Asia WGS AF: 0.478 AC: 1663 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.79
CADD	Benign	4.7
DANN	Benign	0.65

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: rs7762400; hg19: chr6-70445634;