chr16-343342-T-C

Position:

• chr16-343342-T-C

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_003502.4(AXIN1):​c.878+2806A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.917 in 152,244 control chromosomes in the GnomAD database, including 64,245 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 0.92 (64245 hom., cov: 32)
• Consequence: AXIN1 NM_003502.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.89

Genes affected

AXIN1 (HGNC:903): (axin 1) This gene encodes a cytoplasmic protein which contains a regulation of G-protein signaling (RGS) domain and a dishevelled and axin (DIX) domain. The encoded protein interacts with adenomatosis polyposis coli, catenin beta-1, glycogen synthase kinase 3 beta, protein phosphate 2, and itself. This protein functions as a negative regulator of the wingless-type MMTV integration site family, member 1 (WNT) signaling pathway and can induce apoptosis. The crystal structure of a portion of this protein, alone and in a complex with other proteins, has been resolved. Mutations in this gene have been associated with hepatocellular carcinoma, hepatoblastomas, ovarian endometriod adenocarcinomas, and medullablastomas. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

AXIN1 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.977 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
AXIN1	NM_003502.4	c.878+2806A>G		intron_variant		ENST00000262320.8	NP_003493.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
AXIN1	ENST00000262320.8	c.878+2806A>G		intron_variant		1	NM_003502.4	ENSP00000262320.3
AXIN1	ENST00000354866.7	c.878+2806A>G		intron_variant		1		ENSP00000346935.3
AXIN1	ENST00000461023.5	n.175+2806A>G		intron_variant		2
AXIN1	ENST00000481769.1	n.305+9027A>G		intron_variant		3

Frequencies

GnomAD3 genomes AF: 0.917 AC: 139525 AN: 152126 Hom.: 64183 Cov.: 32

Gnomad AFR AF: 0.978

Gnomad AMI AF: 0.910

Gnomad AMR AF: 0.899

Gnomad ASJ AF: 0.794

Gnomad EAS AF: 1.00

Gnomad SAS AF: 0.960

Gnomad FIN AF: 0.888

Gnomad MID AF: 0.775

Gnomad NFE AF: 0.887

Gnomad OTH AF: 0.892

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

GnomAD4 genome AF: 0.917 AC: 139649 AN: 152244 Hom.: 64245 Cov.: 32 AF XY: 0.917 AC XY: 68255 AN XY: 74418

Gnomad4 AFR AF: 0.978

Gnomad4 AMR AF: 0.899

Gnomad4 ASJ AF: 0.794

Gnomad4 EAS AF: 1.00

Gnomad4 SAS AF: 0.959

Gnomad4 FIN AF: 0.888

Gnomad4 NFE AF: 0.887

Gnomad4 OTH AF: 0.892

Alfa AF: 0.903 Hom.: 14306

Bravo AF: 0.921

Asia WGS AF: 0.980 AC: 3406 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.30
DANN	Benign	0.29

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

Publications

LitVar

Other links and lift over

dbSNP: rs395901; hg19: chr16-393342;