rs11634474

Variant names:

• chr15-74823843-C-A
• rs11634474
• NM_021819.3:c.1323+161C>A

Your query was ambiguous. Multiple possible variants found:

• chr15-74823843-C-A
• chr15-74823843-C-G

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_021819.3(LMAN1L):​c.1323+161C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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: not found (cov: 31)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: LMAN1L NM_021819.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.384
• Publications: 17 publications found

Genes affected

LMAN1L (HGNC:6632): (lectin, mannose binding 1 like) This gene encodes a mannose-binding type 1 transmembrane protein that contains an N-terminal lectin-like carbohydrate recognition domain. The encoded protein is similar in structure to lectins found in leguminous plants. This lectin is thought to transport newly synthesized glycoproteins from the endoplasmic reticulum (ER) to the ER-Golgi intermediate compartment. [provided by RefSeq, Jan 2017]

ENSG00000261606 (HGNC:):

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_021819.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LMAN1L	NM_021819.3	MANE Select	c.1323+161C>A		intron	N/A	NP_068591.2	Q9HAT1-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LMAN1L	ENST00000309664.10	TSL:1 MANE Select	c.1323+161C>A		intron	N/A	ENSP00000310431.5	Q9HAT1-1
	LMAN1L	ENST00000379709.7	TSL:1	c.1287+161C>A		intron	N/A	ENSP00000369031.3	Q9HAT1-3
	LMAN1L	ENST00000947251.1		c.1383+161C>A		intron	N/A	ENSP00000617310.1

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Data not reliable, filtered out with message: AC0;AS_VQSR AF: 0.00 AC: 0 AN: 583322 Hom.: 0 Cov.: 8 AF XY: 0.00 AC XY: 0 AN XY: 302418

African (AFR) AF: 0.00 AC: 0 AN: 15090

American (AMR) AF: 0.00 AC: 0 AN: 21214

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 14676

East Asian (EAS) AF: 0.00 AC: 0 AN: 32088

South Asian (SAS) AF: 0.00 AC: 0 AN: 50148

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 30714

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 2240

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 386674

Other (OTH) AF: 0.00 AC: 0 AN: 30478

GnomAD4 genome Cov.: 31

Alfa AF: 0.00 Hom.: 1894

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	8.8
DANN	Benign	0.13
PhyloP100		0.38

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.17		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs11634474; hg19: chr15-75116184;