rs10067856

chr5-109712432-C-T

Variant summary

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

The NM_002372.4(MAN2A1):c.136-1088C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0987 in 152,170 control chromosomes in the GnomAD database, including 1,025 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 0.099 (1025 hom., cov: 32)
• Consequence: MAN2A1 NM_002372.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.178

Genes affected

MAN2A1 (HGNC:6824): (mannosidase alpha class 2A member 1) This gene encodes a glycosyl hydrolase that localizes to the Golgi and catalyzes the final hydrolytic step in the asparagine-linked oligosaccharide (N-glycan) maturation pathway. Mutations in the mouse homolog of this gene have been shown to cause a systemic autoimmune disease similar to human systemic lupus erythematosus. [provided by RefSeq, Dec 2013]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.201 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MAN2A1	NM_002372.4	c.136-1088C>T		intron_variant		ENST00000261483.5
MAN2A1	XM_011543395.4	c.136-1088C>T		intron_variant
MAN2A1	XM_017009472.2	c.-12-1088C>T		intron_variant
MAN2A1	XR_007058604.1	n.627-1088C>T		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MAN2A1	ENST00000261483.5	c.136-1088C>T		intron_variant		1	NM_002372.4	P1

Frequencies

GnomAD3 genomes AF: 0.0986 AC: 14992 AN: 152052 Hom.: 1020 Cov.: 32

Gnomad AFR AF: 0.204

Gnomad AMI AF: 0.0175

Gnomad AMR AF: 0.0513

Gnomad ASJ AF: 0.0757

Gnomad EAS AF: 0.0279

Gnomad SAS AF: 0.0209

Gnomad FIN AF: 0.0586

Gnomad MID AF: 0.0696

Gnomad NFE AF: 0.0650

Gnomad OTH AF: 0.0860

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

GnomAD4 genome AF: 0.0987 AC: 15020 AN: 152170 Hom.: 1025 Cov.: 32 AF XY: 0.0957 AC XY: 7121 AN XY: 74418

Gnomad4 AFR AF: 0.204

Gnomad4 AMR AF: 0.0512

Gnomad4 ASJ AF: 0.0757

Gnomad4 EAS AF: 0.0279

Gnomad4 SAS AF: 0.0211

Gnomad4 FIN AF: 0.0586

Gnomad4 NFE AF: 0.0650

Gnomad4 OTH AF: 0.0851

Alfa AF: 0.0761 Hom.: 272

Bravo AF: 0.103

Asia WGS AF: 0.0400 AC: 139 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
Cadd	Benign	2.5
Dann	Benign	0.82

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: rs10067856; hg19: chr5-109048133;