chr10-122736447-A-T

Variant names:

• chr10-122736447-A-T
• rs2421125
• ENST00000636837.3:n.630+1787A>T

Variant summary

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

The ENST00000636837.3(DMBT1L1):​n.630+1787A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.394 in 151,950 control chromosomes in the GnomAD database, including 12,502 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 0.39 (12502 hom., cov: 32)
• Consequence: DMBT1L1 ENST00000636837.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.27
• Publications: 1 publications found

Genes affected

DMBT1L1 (HGNC:49497): (deleted in malignant brain tumors 1 like 1 (pseudogene))

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.0).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.509 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000636837.3. 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

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DMBT1L1	ENST00000636837.3	TSL:6	n.630+1787A>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.394 AC: 59838 AN: 151832 Hom.: 12457 Cov.: 32

Gnomad AFR AF: 0.514

Gnomad AMI AF: 0.422

Gnomad AMR AF: 0.429

Gnomad ASJ AF: 0.391

Gnomad EAS AF: 0.512

Gnomad SAS AF: 0.440

Gnomad FIN AF: 0.270

Gnomad MID AF: 0.396

Gnomad NFE AF: 0.320

Gnomad OTH AF: 0.400

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

GnomAD4 genome AF: 0.394 AC: 59931 AN: 151950 Hom.: 12502 Cov.: 32 AF XY: 0.395 AC XY: 29304 AN XY: 74264

African (AFR) AF: 0.515 AC: 21320 AN: 41394

American (AMR) AF: 0.429 AC: 6556 AN: 15268

Ashkenazi Jewish (ASJ) AF: 0.391 AC: 1357 AN: 3470

East Asian (EAS) AF: 0.513 AC: 2647 AN: 5160

South Asian (SAS) AF: 0.439 AC: 2113 AN: 4812

European-Finnish (FIN) AF: 0.270 AC: 2850 AN: 10572

Middle Eastern (MID) AF: 0.405 AC: 119 AN: 294

European-Non Finnish (NFE) AF: 0.320 AC: 21745 AN: 67962

Other (OTH) AF: 0.398 AC: 839 AN: 2106

Alfa AF: 0.362 Hom.: 1318

Bravo AF: 0.411

Asia WGS AF: 0.464 AC: 1609 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	0.065
DANN	Benign	0.41
PhyloP100		-2.3

Splicing

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

Other links and lift over

dbSNP: rs2421125; hg19: chr10-124495963;