rs55915411

Variant names:

• chr1-68486881-AACACACACACACACACACACACACACAC-A
• rs55915411
• NM_001114120.3:c.769+28_769+55delGTGTGTGTGTGTGTGTGTGTGTGTGTGT

Your query was ambiguous. Multiple possible variants found:

• chr1-68486881-AACACACACACACACACACACACACACAC-A
• chr1-68486881-AACACACACACACACACACACACACACAC-AAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACACACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACACACACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACACACACACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACACACACACACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACACACACACACACACACACACACACAC
• chr1-68486881-AACACACACACACACACACACACACACAC-AACACACACACACACACACACACACACACACACACACACACACACAC

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 0P and 0B.

The NM_001114120.3(DEPDC1):​c.769+28_769+55delGTGTGTGTGTGTGTGTGTGTGTGTGTGT variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000000967 in 1,033,714 control chromosomes in the GnomAD database, with no homozygous occurrence. It is difficult to determine the true allele frequency of this variant because it is of type DEL_BIG, and the frequency of such variant types in population databases may be underestimated and unreliable. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.0 (0 hom., cov: 0)
  • Exomes 𝑓: 9.7e-7 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: DEPDC1 NM_001114120.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 2.95
• Publications: 0 publications found

Genes affected

DEPDC1 (HGNC:22949): (DEP domain containing 1) Predicted to enable GTPase activator activity. Involved in negative regulation of transcription, DNA-templated. Located in nucleus. Part of transcription repressor complex. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001114120.3. 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
	DEPDC1	NM_001114120.3	MANE Select	c.769+28_769+55delGTGTGTGTGTGTGTGTGTGTGTGTGTGT		intron	N/A	NP_001107592.1	Q5TB30-5
	DEPDC1	NM_017779.6		c.769+28_769+55delGTGTGTGTGTGTGTGTGTGTGTGTGTGT		intron	N/A	NP_060249.2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DEPDC1	ENST00000456315.7	TSL:1 MANE Select	c.769+28_769+55delGTGTGTGTGTGTGTGTGTGTGTGTGTGT		intron	N/A	ENSP00000412292.2	Q5TB30-5
	DEPDC1	ENST00000370966.9	TSL:1	c.769+28_769+55delGTGTGTGTGTGTGTGTGTGTGTGTGTGT		intron	N/A	ENSP00000360005.5	Q5TB30-2
	DEPDC1	ENST00000489862.1	TSL:1	n.472+28_472+55delGTGTGTGTGTGTGTGTGTGTGTGTGTGT		intron	N/A	ENSP00000436464.1	H0YES2

Frequencies

GnomAD3 genomes AF: 0.00 AC: 0 AN: 143644 Hom.: 0 Cov.: 0

Gnomad AFR AF: 0.00

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.00

Gnomad OTH AF: 0.00

GnomAD4 exome AF: 9.67e-7 AC: 1 AN: 1033714 Hom.: 0 AF XY: 0.00000198 AC XY: 1 AN XY: 505512

⚠️ The allele balance in gnomAD version 4 Exomes is significantly skewed from the expected value of 0.5.

African (AFR) AF: 0.00 AC: 0 AN: 22598

American (AMR) AF: 0.00 AC: 0 AN: 17934

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 15442

East Asian (EAS) AF: 0.00 AC: 0 AN: 30270

South Asian (SAS) AF: 0.0000331 AC: 1 AN: 30200

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 41466

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 3316

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 830150

Other (OTH) AF: 0.00 AC: 0 AN: 42338

⚠️ The allele balance in gnomAD4 Exomes is highly skewed from 0.5 (p-value = 0), which strongly suggests a high chance of mosaicism in these individuals.

GnomAD4 genome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 143644 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 69500

African (AFR) AF: 0.00 AC: 0 AN: 38842

American (AMR) AF: 0.00 AC: 0 AN: 14172

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 3350

East Asian (EAS) AF: 0.00 AC: 0 AN: 4854

South Asian (SAS) AF: 0.00 AC: 0 AN: 4386

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 9446

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 306

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 65430

Other (OTH) AF: 0.00 AC: 0 AN: 1966

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		2.9

Splicing

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

Other links and lift over

dbSNP: rs55915411; hg19: chr1-68952564;