rs1945502699

Variant names:

• chr11-125956935-C-G
• rs1945502699
• NM_001378964.1:c.*4007G>C

Your query was ambiguous. Multiple possible variants found:

• chr11-125956935-C-G
• chr11-125956935-C-T

Variant summary

Our verdict is Benign. The variant received -8 ACMG points: 0P and 8B. BP4_Strong BS2

The NM_001378964.1(CDON):​c.*4007G>C variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0000144 in 695,254 control chromosomes in the GnomAD database, with no homozygous occurrence. 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: not found (cov: 33)
  • Exomes 𝑓: 0.000014 (0 hom.)
• Consequence: CDON NM_001378964.1 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.03
• Publications: 0 publications found

Genes affected

CDON (HGNC:17104): (cell adhesion associated, oncogene regulated) This gene encodes a cell surface receptor that is a member of the immunoglobulin superfamily. The encoded protein contains three fibronectin type III domains and five immunoglobulin-like C2-type domains. This protein is a member of a cell-surface receptor complex that mediates cell-cell interactions between muscle precursor cells and positively regulates myogenesis. [provided by RefSeq, Aug 2011]

VSIG10L2 (HGNC:27879): (V-set and immunoglobulin domain containing 10 like 2) Predicted to enable cell adhesion molecule binding activity. Predicted to be involved in cell-cell adhesion. Predicted to be active in cell-cell junction. Predicted to be integral component of plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Benign. The variant received -8 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BS2: High AC in GnomAdExome4 at 10 AD gene.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CDON	NM_001378964.1	c.*4007G>C		3_prime_UTR_variant	Exon 20 of 20	ENST00000531738.6	NP_001365893.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CDON	ENST00000531738.6	c.*4007G>C		3_prime_UTR_variant	Exon 20 of 20	1	NM_001378964.1	ENSP00000432901.2
CDON	ENST00000392693.7	c.*4007G>C		3_prime_UTR_variant	Exon 20 of 20	1		ENSP00000376458.3
CDON	ENST00000684078.1	c.*4007G>C		3_prime_UTR_variant	Exon 20 of 20			ENSP00000507318.1
VSIG10L2	ENST00000638636.2	c.*1021C>G		3_prime_UTR_variant	Exon 10 of 10	5		ENSP00000491467.1

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome AF: 0.0000144 AC: 10 AN: 695254 Hom.: 0 Cov.: 9 AF XY: 0.0000216 AC XY: 7 AN XY: 323600

African (AFR) AF: 0.00 AC: 0 AN: 13132

American (AMR) AF: 0.00 AC: 0 AN: 832

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 4198

East Asian (EAS) AF: 0.00 AC: 0 AN: 2960

South Asian (SAS) AF: 0.00 AC: 0 AN: 13744

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 224

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 1348

European-Non Finnish (NFE) AF: 0.0000141 AC: 9 AN: 636078

Other (OTH) AF: 0.0000440 AC: 1 AN: 22738

GnomAD4 genome Cov.: 33

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	0.20
DANN	Benign	0.63
PhyloP100		-2.0

Splicing

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

Other links and lift over

dbSNP: rs1945502699; hg19: chr11-125826830;