rs4736078

Variant names:

• chr8-138862873-G-A
• rs4736078
• NM_152888.3:c.658+14877C>T

Your query was ambiguous. Multiple possible variants found:

• chr8-138862873-G-A
• chr8-138862873-G-C
• chr8-138862873-G-T

Variant summary

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

The NM_152888.3(COL22A1):​c.658+14877C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.685 in 151,704 control chromosomes in the GnomAD database, including 37,718 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 0.68 (37718 hom., cov: 29)
• Consequence: COL22A1 NM_152888.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.36
• Publications: 4 publications found

Genes affected

COL22A1 (HGNC:22989): (collagen type XXII alpha 1 chain) This gene encodes member of the collagen family which is thought to contribute to the stabilization of myotendinous junctions and strengthen skeletal muscle attachments during contractile activity. It belongs to the fibril-associated collagens with interrupted triple helix (FACIT) subset of the collagen superfamily, which associate with collagen fibers through their C-terminal collagenous domains and mediate protein-protein interactions through their N-terminal noncollagenous domains. The encoded protein is deposited in the basement membrane zone of the myotendinous junction which is present only at the tissue junctions of muscles, tendons, the heart, articular cartilage, and skin. A knockdown of the orthologous zebrafish gene induces a muscular dystrophy by disruption of the myotendinous junction. [provided by RefSeq, May 2017]

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 (EAS) allele frequency at 95% confidence interval = 0.943 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
COL22A1	NM_152888.3	c.658+14877C>T		intron_variant	Intron 3 of 64	ENST00000303045.11	NP_690848.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
COL22A1	ENST00000303045.11	c.658+14877C>T		intron_variant	Intron 3 of 64	1	NM_152888.3	ENSP00000303153.6

Frequencies

GnomAD3 genomes AF: 0.685 AC: 103817 AN: 151586 Hom.: 37718 Cov.: 29

Gnomad AFR AF: 0.418

Gnomad AMI AF: 0.791

Gnomad AMR AF: 0.739

Gnomad ASJ AF: 0.774

Gnomad EAS AF: 0.966

Gnomad SAS AF: 0.869

Gnomad FIN AF: 0.851

Gnomad MID AF: 0.723

Gnomad NFE AF: 0.767

Gnomad OTH AF: 0.697

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

GnomAD4 genome AF: 0.685 AC: 103848 AN: 151704 Hom.: 37718 Cov.: 29 AF XY: 0.693 AC XY: 51390 AN XY: 74156

African (AFR) AF: 0.418 AC: 17203 AN: 41198

American (AMR) AF: 0.739 AC: 11280 AN: 15258

Ashkenazi Jewish (ASJ) AF: 0.774 AC: 2681 AN: 3462

East Asian (EAS) AF: 0.966 AC: 4967 AN: 5144

South Asian (SAS) AF: 0.869 AC: 4176 AN: 4804

European-Finnish (FIN) AF: 0.851 AC: 8983 AN: 10560

Middle Eastern (MID) AF: 0.729 AC: 213 AN: 292

European-Non Finnish (NFE) AF: 0.767 AC: 52159 AN: 67970

Other (OTH) AF: 0.696 AC: 1468 AN: 2108

Alfa AF: 0.739 Hom.: 126298

Bravo AF: 0.664

Asia WGS AF: 0.853 AC: 2966 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.38
DANN	Benign	0.60
PhyloP100		-1.4
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: rs4736078; hg19: chr8-139875116; COSMIC: COSV57362841;