17-50201443-TCTTGGC-T

Position:

• chr17-50201443-TCTTGGC-T

Variant summary

Our verdict is Uncertain significance. Variant got 5 ACMG points: 5P and 0B. PM1 PM2 PP5

The NM_000088.4(COL1A1):​c.65_70delGCCAAG​(p.Gly22_Gln23del) variant causes a disruptive inframe deletion change. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Pathogenic (no stars).

• Frequency: Genomes: not found (cov: 33)
• Consequence: COL1A1 NM_000088.4 disruptive_inframe_deletion
• Clinical Significance: Pathogenic no assertion criteria provided P:1
• Conservation: PhyloP100: 7.01

Genes affected

COL1A1 (HGNC:2197): (collagen type I alpha 1 chain) This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish, Feb 2008]

COL1A1 (HGNC:):

ACMG classification

Verdict is Uncertain_significance. Variant got 5 ACMG points.

• PM1: In a signal_peptide (size 21) in uniprot entity CO1A1_HUMAN there are 5 pathogenic changes around while only 0 benign (100%) in NM_000088.4
• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant 17-50201443-TCTTGGC-T is Pathogenic according to our data. Variant chr17-50201443-TCTTGGC-T is described in ClinVar as [Pathogenic]. Clinvar id is 425636.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr17-50201443-TCTTGGC-T is described in Lovd as [Pathogenic]. Variant chr17-50201443-TCTTGGC-T is described in Lovd as [Pathogenic].

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
COL1A1	NM_000088.4	c.65_70delGCCAAG	p.Gly22_Gln23del	disruptive_inframe_deletion	1/51	ENST00000225964.10	NP_000079.2
COL1A1	XM_011524341.2	c.65_70delGCCAAG	p.Gly22_Gln23del	disruptive_inframe_deletion	1/48		XP_011522643.1
COL1A1	XM_005257058.5	c.65_70delGCCAAG	p.Gly22_Gln23del	disruptive_inframe_deletion	1/49		XP_005257115.2
COL1A1	XM_005257059.5	c.65_70delGCCAAG	p.Gly22_Gln23del	disruptive_inframe_deletion	1/38		XP_005257116.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
COL1A1	ENST00000225964.10	c.65_70delGCCAAG	p.Gly22_Gln23del	disruptive_inframe_deletion	1/51	1	NM_000088.4	ENSP00000225964.6
COL1A1	ENST00000474644.1	n.184_189delGCCAAG		non_coding_transcript_exon_variant	1/4	3
ENSG00000249406	ENST00000509943.2	n.59+1511_59+1516delTTGGCC		intron_variant		3

Frequencies

GnomAD3 genomes Cov.: 33

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

GnomAD4 genome Cov.: 33

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: no assertion criteria provided

Submissions by phenotype

Osteogenesis imperfecta type III Pathogenic:1

Pathogenic, no assertion criteria provided

clinical testing

Department of Medical Sciences, Uppsala University

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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: rs1114167409; hg19: chr17-48278804;