6-11334421-C-G

Variant names:

• chr6-11334421-C-G
• rs760678
• ENST00000448183.6:n.-152-28266G>C

Variant summary

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

The ENST00000448183.6(NEDD9):​n.-152-28266G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.689 in 152,100 control chromosomes in the GnomAD database, including 37,100 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 0.69 (37100 hom., cov: 32)
  • Failed GnomAD Quality Control
• Consequence: NEDD9 ENST00000448183.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.443
• Publications: 15 publications found

Genes affected

NEDD9 (HGNC:7733): (neural precursor cell expressed, developmentally down-regulated 9) The protein encoded by this gene is a member of the CRK-associated substrates family. Members of this family are adhesion docking molecules that mediate protein-protein interactions for signal transduction pathways. This protein is a focal adhesion protein that acts as a scaffold to regulate signaling complexes important in cell attachment, migration and invasion as well as apoptosis and the cell cycle. This protein has also been reported to have a role in cancer metastasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]

LOC105374925 (HGNC:):

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.842 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LOC105374925	XR_007059445.1	n.18851C>G		non_coding_transcript_exon_variant	Exon 4 of 4
LOC105374925	XR_007059446.1	n.18480C>G		non_coding_transcript_exon_variant	Exon 7 of 7
LOC105374925	XR_007059447.1	n.17197C>G		non_coding_transcript_exon_variant	Exon 7 of 7

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
NEDD9	ENST00000448183.6	n.-152-28266G>C		intron_variant	Intron 1 of 9	1		ENSP00000395237.2
NEDD9	ENST00000504387.5	c.-152-28266G>C		intron_variant	Intron 1 of 7	2		ENSP00000422871.1
NEDD9	ENST00000397378.7	c.-153+80G>C		intron_variant	Intron 2 of 3	3		ENSP00000380534.3

Frequencies

GnomAD3 genomes AF: 0.689 AC: 104714 AN: 151984 Hom.: 37039 Cov.: 32

Gnomad AFR AF: 0.849

Gnomad AMI AF: 0.749

Gnomad AMR AF: 0.720

Gnomad ASJ AF: 0.702

Gnomad EAS AF: 0.701

Gnomad SAS AF: 0.721

Gnomad FIN AF: 0.529

Gnomad MID AF: 0.634

Gnomad NFE AF: 0.605

Gnomad OTH AF: 0.682

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

GnomAD4 genome AF: 0.689 AC: 104836 AN: 152100 Hom.: 37100 Cov.: 32 AF XY: 0.686 AC XY: 51028 AN XY: 74342

African (AFR) AF: 0.850 AC: 35263 AN: 41506

American (AMR) AF: 0.721 AC: 11015 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.702 AC: 2435 AN: 3470

East Asian (EAS) AF: 0.702 AC: 3632 AN: 5176

South Asian (SAS) AF: 0.722 AC: 3480 AN: 4822

European-Finnish (FIN) AF: 0.529 AC: 5580 AN: 10544

Middle Eastern (MID) AF: 0.637 AC: 186 AN: 292

European-Non Finnish (NFE) AF: 0.605 AC: 41130 AN: 67990

Other (OTH) AF: 0.679 AC: 1433 AN: 2110

Alfa AF: 0.646 Hom.: 3783

Bravo AF: 0.711

Asia WGS AF: 0.713 AC: 2479 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	0.45
DANN	Benign	0.31
PhyloP100		-0.44
Mutation Taster		=100/0	polymorphism (auto)

Splicing

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

Other links and lift over

dbSNP: rs760678; hg19: chr6-11334654;