chr1-92936994-C-T

Variant names:

• chr1-92936994-C-T
• rs17380908
• NM_001006605.5:c.54+24382G>A

Variant summary

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

The NM_001006605.5(DIPK1A):​c.54+24382G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.35 in 152,048 control chromosomes in the GnomAD database, including 9,757 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 0.35 (9757 hom., cov: 32)
• Consequence: DIPK1A NM_001006605.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.189
• Publications: 7 publications found

Genes affected

DIPK1A (HGNC:32213): (divergent protein kinase domain 1A) This gene encodes a member of the FAM69 family of cysteine-rich type II transmembrane proteins. These proteins localize to the endoplasmic reticulum but their specific functions are unknown. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.38 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001006605.5. 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
	DIPK1A	NM_001006605.5	MANE Select	c.54+24382G>A		intron	N/A	NP_001006606.2
	DIPK1A	NM_001252269.2		c.54+24382G>A		intron	N/A	NP_001239198.1
	DIPK1A	NM_001252270.2		c.54+24382G>A		intron	N/A	NP_001239199.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DIPK1A	ENST00000370310.5	TSL:2 MANE Select	c.54+24382G>A		intron	N/A	ENSP00000359333.4
	DIPK1A	ENST00000615519.4	TSL:1	c.54+24382G>A		intron	N/A	ENSP00000483279.1
	DIPK1A	ENST00000613902.4	TSL:4	c.54+24382G>A		intron	N/A	ENSP00000484866.1

Frequencies

GnomAD3 genomes AF: 0.350 AC: 53141 AN: 151930 Hom.: 9746 Cov.: 32

Gnomad AFR AF: 0.384

Gnomad AMI AF: 0.366

Gnomad AMR AF: 0.327

Gnomad ASJ AF: 0.239

Gnomad EAS AF: 0.0542

Gnomad SAS AF: 0.194

Gnomad FIN AF: 0.385

Gnomad MID AF: 0.339

Gnomad NFE AF: 0.367

Gnomad OTH AF: 0.365

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

GnomAD4 genome AF: 0.350 AC: 53194 AN: 152048 Hom.: 9757 Cov.: 32 AF XY: 0.346 AC XY: 25681 AN XY: 74318

African (AFR) AF: 0.385 AC: 15941 AN: 41448

American (AMR) AF: 0.327 AC: 4993 AN: 15278

Ashkenazi Jewish (ASJ) AF: 0.239 AC: 829 AN: 3466

East Asian (EAS) AF: 0.0545 AC: 283 AN: 5188

South Asian (SAS) AF: 0.194 AC: 931 AN: 4808

European-Finnish (FIN) AF: 0.385 AC: 4067 AN: 10562

Middle Eastern (MID) AF: 0.350 AC: 103 AN: 294

European-Non Finnish (NFE) AF: 0.367 AC: 24952 AN: 67984

Other (OTH) AF: 0.361 AC: 763 AN: 2112

Alfa AF: 0.345 Hom.: 1437

Bravo AF: 0.347

Asia WGS AF: 0.184 AC: 641 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	8.3
DANN	Benign	0.68
PhyloP100		0.19
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: rs17380908; hg19: chr1-93402551;