rs9296736

chr6-54059899-T-C

Variant summary

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

The ENST00000514921.5(MLIP):c.63+40808T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.512 in 152,088 control chromosomes in the GnomAD database, including 23,869 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 0.51 (23869 hom., cov: 44)
• Consequence: MLIP ENST00000514921.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.130

Genes affected

MLIP (HGNC:21355): (muscular LMNA interacting protein) Predicted to enable lamin binding activity and transcription corepressor activity. Predicted to be involved in negative regulation of cardiac muscle hypertrophy in response to stress; negative regulation of transcription by RNA polymerase II; and positive regulation of transcription by RNA polymerase II. Predicted to be located in nuclear lumen. Predicted to be active in PML body; nuclear envelope; and sarcolemma. [provided by Alliance of Genome Resources, Apr 2022]

MLIP-AS1 (HGNC:40963): (MLIP antisense RNA 1)

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.61).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.683 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MLIP	NM_001281746.2	c.63+40808T>C		intron_variant
MLIP	NM_138569.3	c.63+40808T>C		intron_variant
MLIP	XM_005249476.6	c.63+40808T>C		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MLIP	ENST00000514921.5	c.63+40808T>C		intron_variant		1
MLIP	ENST00000274897.9	c.63+40808T>C		intron_variant		2		P1
MLIP	ENST00000370877.6	c.63+40808T>C		intron_variant		5

Frequencies

GnomAD3 genomes AF: 0.513 AC: 77891 AN: 151970 Hom.: 23875 Cov.: 44

Gnomad AFR AF: 0.165

Gnomad AMI AF: 0.696

Gnomad AMR AF: 0.482

Gnomad ASJ AF: 0.644

Gnomad EAS AF: 0.487

Gnomad SAS AF: 0.576

Gnomad FIN AF: 0.700

Gnomad MID AF: 0.547

Gnomad NFE AF: 0.688

Gnomad OTH AF: 0.554

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

GnomAD4 genome AF: 0.512 AC: 77887 AN: 152088 Hom.: 23869 Cov.: 44 AF XY: 0.514 AC XY: 38220 AN XY: 74362

Gnomad4 AFR AF: 0.165

Gnomad4 AMR AF: 0.482

Gnomad4 ASJ AF: 0.644

Gnomad4 EAS AF: 0.487

Gnomad4 SAS AF: 0.577

Gnomad4 FIN AF: 0.700

Gnomad4 NFE AF: 0.688

Gnomad4 OTH AF: 0.548

Alfa AF: 0.632 Hom.: 11653

Bravo AF: 0.480

Asia WGS AF: 0.477 AC: 1659 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.61
Cadd	Benign	7.7
Dann	Benign	0.80

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: rs9296736; hg19: chr6-53924697;