NM_001171038.2:c.562+78T>C

Variant names:

• chrX-1630017-T-C
• rs28675287
• NM_001171038.2:c.562+78T>C

Variant summary

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

The NM_001171038.2(ASMT):​c.562+78T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.148 in 1,277,486 control chromosomes in the GnomAD database, including 15,282 homozygotes. There are 97,639 hemizygotes in GnomAD. 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 0.13 (1553 hom., 10212 hem., cov: 32)
  • Exomes 𝑓: 0.15 (13729 hom. 87427 hem.)
• Consequence: ASMT NM_001171038.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.59
• Publications: 0 publications found

Genes affected

ASMT (HGNC:750): (acetylserotonin O-methyltransferase) This gene belongs to the methyltransferase superfamily, and is located in the pseudoautosomal region (PAR) at the end of the short arms of the X and Y chromosomes. The encoded enzyme catalyzes the final reaction in the synthesis of melatonin, and is abundant in the pineal gland. Alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Jan 2010]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.39 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001171038.2. 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
	ASMT	NM_001171038.2	MANE Select	c.562+78T>C		intron	N/A	NP_001164509.1	P46597-3
	ASMT	NM_001416525.1		c.562+78T>C		intron	N/A	NP_001403454.1	X5D2A4
	ASMT	NM_001171039.1		c.562+78T>C		intron	N/A	NP_001164510.1	X5D784

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ASMT	ENST00000381241.9	TSL:1 MANE Select	c.562+78T>C		intron	N/A	ENSP00000370639.3	P46597-3
	ASMT	ENST00000381229.9	TSL:1	c.562+78T>C		intron	N/A	ENSP00000370627.4	P46597-1
	ASMT	ENST00000381233.8	TSL:1	c.562+78T>C		intron	N/A	ENSP00000370631.3	P46597-2

Frequencies

GnomAD3 genomes AF: 0.135 AC: 20432 AN: 151812 Hom.: 1552 Cov.: 32

Gnomad AFR AF: 0.0836

Gnomad AMI AF: 0.135

Gnomad AMR AF: 0.142

Gnomad ASJ AF: 0.225

Gnomad EAS AF: 0.405

Gnomad SAS AF: 0.187

Gnomad FIN AF: 0.158

Gnomad MID AF: 0.209

Gnomad NFE AF: 0.131

Gnomad OTH AF: 0.148

GnomAD4 exome AF: 0.150 AC: 168712 AN: 1125556 Hom.: 13729 AF XY: 0.152 AC XY: 87427 AN XY: 573548

African (AFR) AF: 0.0878 AC: 2403 AN: 27384

American (AMR) AF: 0.137 AC: 6077 AN: 44282

Ashkenazi Jewish (ASJ) AF: 0.236 AC: 5656 AN: 23942

East Asian (EAS) AF: 0.364 AC: 13869 AN: 38138

South Asian (SAS) AF: 0.192 AC: 15325 AN: 79742

European-Finnish (FIN) AF: 0.154 AC: 8206 AN: 53278

Middle Eastern (MID) AF: 0.228 AC: 1166 AN: 5110

European-Non Finnish (NFE) AF: 0.134 AC: 107645 AN: 804510

Other (OTH) AF: 0.170 AC: 8365 AN: 49170

GnomAD4 genome AF: 0.135 AC: 20436 AN: 151930 Hom.: 1553 Cov.: 32 AF XY: 0.138 AC XY: 10212 AN XY: 74248

African (AFR) AF: 0.0838 AC: 3468 AN: 41382

American (AMR) AF: 0.142 AC: 2163 AN: 15230

Ashkenazi Jewish (ASJ) AF: 0.225 AC: 780 AN: 3464

East Asian (EAS) AF: 0.404 AC: 2092 AN: 5176

South Asian (SAS) AF: 0.185 AC: 891 AN: 4814

European-Finnish (FIN) AF: 0.158 AC: 1670 AN: 10594

Middle Eastern (MID) AF: 0.207 AC: 61 AN: 294

European-Non Finnish (NFE) AF: 0.131 AC: 8872 AN: 67964

Other (OTH) AF: 0.150 AC: 316 AN: 2100

Bravo AF: 0.135

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	1.2
DANN	Benign	0.15
PhyloP100		1.6

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: rs28675287; hg19: chrX-1748910; COSMIC: COSV67110026;