NM_015375.3:c.2603-172_2603-171dupTT

Variant names:

• chr1-205147915-T-TAA
• rs35284794
• NM_015375.3:c.2603-172_2603-171dupTT

Variant summary

Our verdict is Benign. Variant got -8 ACMG points: 0P and 8B. BS1 BS2

The NM_015375.3(DSTYK):​c.2603-172_2603-171dupTT variant causes a intron change involving the alteration of a non-conserved nucleotide. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.00019 (0 hom., cov: 0)
• Consequence: DSTYK NM_015375.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -3.28

Genes affected

DSTYK (HGNC:29043): (dual serine/threonine and tyrosine protein kinase) This gene encodes a dual serine/threonine and tyrosine protein kinase which is expressed in multiple tissues. It is thought to function as a regulator of cell death. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]

ACMG classification

Verdict is Benign. Variant got -8 ACMG points.

• BS1: Variant frequency is greater than expected in population amr. gnomad4 allele frequency = 0.000194 (28/144522) while in subpopulation AMR AF= 0.000341 (5/14656). AF 95% confidence interval is 0.000174. There are 0 homozygotes in gnomad4. There are 12 alleles in male gnomad4 subpopulation. Median coverage is 0. This position pass quality control queck.
• BS2: High AC in GnomAd4 at 28 AD gene.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
DSTYK	NM_015375.3	c.2603-172_2603-171dupTT		intron_variant	Intron 12 of 12	ENST00000367162.8	NP_056190.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
DSTYK	ENST00000367162.8	c.2603-171_2603-170insTT		intron_variant	Intron 12 of 12	1	NM_015375.3	ENSP00000356130.3
DSTYK	ENST00000367161.7	c.2468-171_2468-170insTT		intron_variant	Intron 11 of 11	1		ENSP00000356129.3

Frequencies

GnomAD3 genomes AF: 0.000187 AC: 27 AN: 144442 Hom.: 0 Cov.: 0

Gnomad AFR AF: 0.0000528

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.000342

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.000219

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.000270

Gnomad OTH AF: 0.00

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

GnomAD4 genome AF: 0.000194 AC: 28 AN: 144522 Hom.: 0 Cov.: 0 AF XY: 0.000171 AC XY: 12 AN XY: 70184

Gnomad4 AFR AF: 0.0000789

Gnomad4 AMR AF: 0.000341

Gnomad4 ASJ AF: 0.00

Gnomad4 EAS AF: 0.00

Gnomad4 SAS AF: 0.00

Gnomad4 FIN AF: 0.000219

Gnomad4 NFE AF: 0.000271

Gnomad4 OTH AF: 0.00

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs35284794; hg19: chr1-205117043;