NM_201544.4:c.*2846_*2849delAAAA

Variant names:

• chr1-236550992-TAAAA-T
• rs55866014
• NM_201544.4:c.*2846_*2849delAAAA

Variant summary

Our verdict is Uncertain significance. The variant received 2 ACMG points: 2P and 0B. PM2

The NM_201544.4(LGALS8):​c.*2846_*2849delAAAA variant causes a 3 prime UTR change. The variant allele was found at a frequency of 0.000051 in 1,117,450 control chromosomes in the GnomAD database, with no homozygous occurrence. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: not found (cov: 0)
  • Exomes 𝑓: 0.000051 (0 hom.)
• Consequence: LGALS8 NM_201544.4 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 4.48
• Publications: 0 publications found

Genes affected

LGALS8 (HGNC:6569): (galectin 8) This gene encodes a member of the galectin family. Galectins are beta-galactoside-binding animal lectins with conserved carbohydrate recognition domains. The galectins have been implicated in many essential functions including development, differentiation, cell-cell adhesion, cell-matrix interaction, growth regulation, apoptosis, and RNA splicing. This gene is widely expressed in tumoral tissues and seems to be involved in integrin-like cell interactions. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

HEATR1 (HGNC:25517): (HEAT repeat containing 1) Enables RNA binding activity. Involved in positive regulation of rRNA processing and positive regulation of transcription by RNA polymerase I. Located in fibrillar center and mitochondrion. Implicated in pancreatic ductal carcinoma. Biomarker of glioblastoma. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Uncertain_significance. The variant received 2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_201544.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LGALS8	NM_201544.4	MANE Select	c.*2846_*2849delAAAA		3_prime_UTR	Exon 10 of 10	NP_963838.1
	HEATR1	NM_018072.6	MANE Select	c.6347-6_6347-3delTTTT		splice_region intron	N/A	NP_060542.4
	LGALS8	NM_006499.5		c.*2846_*2849delAAAA		3_prime_UTR	Exon 12 of 12	NP_006490.3

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LGALS8	ENST00000366584.9	TSL:1 MANE Select	c.*2846_*2849delAAAA		3_prime_UTR	Exon 10 of 10	ENSP00000355543.4
	LGALS8	ENST00000450372.6	TSL:1	c.*2846_*2849delAAAA		3_prime_UTR	Exon 12 of 12	ENSP00000408657.2
	HEATR1	ENST00000366582.8	TSL:5 MANE Select	c.6347-6_6347-3delTTTT		splice_region intron	N/A	ENSP00000355541.3

Frequencies

GnomAD3 genomes Cov.: 0

GnomAD4 exome AF: 0.0000510 AC: 57 AN: 1117450 Hom.: 0 AF XY: 0.0000432 AC XY: 24 AN XY: 556010

⚠️ The allele balance in gnomAD version 4 Exomes is significantly skewed from the expected value of 0.5.

African (AFR) AF: 0.000115 AC: 3 AN: 26084

American (AMR) AF: 0.000210 AC: 5 AN: 23776

Ashkenazi Jewish (ASJ) AF: 0.0000526 AC: 1 AN: 19014

East Asian (EAS) AF: 0.0000292 AC: 1 AN: 34232

South Asian (SAS) AF: 0.0000491 AC: 3 AN: 61112

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 31246

Middle Eastern (MID) AF: 0.000257 AC: 1 AN: 3890

European-Non Finnish (NFE) AF: 0.0000483 AC: 42 AN: 870040

Other (OTH) AF: 0.0000208 AC: 1 AN: 48056

⚠️ The allele balance in gnomAD4 Exomes is highly skewed from 0.5 (p-value = 0), which strongly suggests a high chance of mosaicism in these individuals.

GnomAD4 genome Cov.: 0

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		4.5

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

Other links and lift over

dbSNP: rs55866014; hg19: chr1-236714292;