NM_052917.4:c.1156+13038T>G

Variant names:

• chr2-154314627-T-G
• rs12693973
• NM_052917.4:c.1156+13038T>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_052917.4(GALNT13):​c.1156+13038T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.193 in 152,080 control chromosomes in the GnomAD database, including 3,295 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 0.19 (3295 hom., cov: 32)
• Consequence: GALNT13 NM_052917.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.803
• Publications: 5 publications found

Genes affected

GALNT13 (HGNC:23242): (polypeptide N-acetylgalactosaminyltransferase 13) The GALNT13 protein is a member of the UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GalNAcT; EC 2.4.1.41) family, which initiate O-linked glycosylation of mucins (see MUC3A, MIM 158371) by the initial transfer of N-acetylgalactosamine (GalNAc) with an alpha-linkage to a serine or threonine residue.[supplied by OMIM, Apr 2004]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.01).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.238 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_052917.4. 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
	GALNT13	NM_052917.4	MANE Select	c.1156+13038T>G		intron	N/A	NP_443149.2
	GALNT13	NM_001376403.1		c.1156+13038T>G		intron	N/A	NP_001363332.1
	GALNT13	NM_001376404.1		c.1156+13038T>G		intron	N/A	NP_001363333.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GALNT13	ENST00000392825.8	TSL:2 MANE Select	c.1156+13038T>G		intron	N/A	ENSP00000376570.3
	GALNT13	ENST00000409237.5	TSL:1	c.1156+13038T>G		intron	N/A	ENSP00000387239.1
	GALNT13	ENST00000431076.5	TSL:1	n.*976+13038T>G		intron	N/A	ENSP00000389447.1

Frequencies

GnomAD3 genomes AF: 0.193 AC: 29305 AN: 151962 Hom.: 3300 Cov.: 32

Gnomad AFR AF: 0.0926

Gnomad AMI AF: 0.356

Gnomad AMR AF: 0.213

Gnomad ASJ AF: 0.244

Gnomad EAS AF: 0.187

Gnomad SAS AF: 0.177

Gnomad FIN AF: 0.204

Gnomad MID AF: 0.370

Gnomad NFE AF: 0.241

Gnomad OTH AF: 0.264

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

GnomAD4 genome AF: 0.193 AC: 29283 AN: 152080 Hom.: 3295 Cov.: 32 AF XY: 0.191 AC XY: 14213 AN XY: 74324

African (AFR) AF: 0.0923 AC: 3834 AN: 41516

American (AMR) AF: 0.213 AC: 3248 AN: 15266

Ashkenazi Jewish (ASJ) AF: 0.244 AC: 848 AN: 3470

East Asian (EAS) AF: 0.187 AC: 964 AN: 5152

South Asian (SAS) AF: 0.177 AC: 852 AN: 4820

European-Finnish (FIN) AF: 0.204 AC: 2155 AN: 10558

Middle Eastern (MID) AF: 0.347 AC: 102 AN: 294

European-Non Finnish (NFE) AF: 0.241 AC: 16408 AN: 67982

Other (OTH) AF: 0.259 AC: 548 AN: 2112

Alfa AF: 0.230 Hom.: 17756

Bravo AF: 0.192

Asia WGS AF: 0.161 AC: 563 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	1.2
DANN	Benign	0.58
PhyloP100		-0.80
Mutation Taster		=100/0	polymorphism (auto)

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: rs12693973; hg19: chr2-155171139;