rs6931735

chr6-135303673-G-Achr6-135303673-G-Cchr6-135303673-G-T

Variant summary

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

The NM_001134831.2(AHI1):c.3427-3115C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.598 in 152,018 control chromosomes in the GnomAD database, including 27,363 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 0.60 (27363 hom., cov: 32)
• Consequence: AHI1 NM_001134831.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.617

Genes affected

AHI1 (HGNC:21575): (Abelson helper integration site 1) This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.648 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
AHI1	NM_001134831.2	c.3427-3115C>T		intron_variant		ENST00000265602.11

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
AHI1	ENST00000265602.11	c.3427-3115C>T		intron_variant		1	NM_001134831.2	P2
	ENST00000444302.1	n.124-1361G>A		intron_variant, non_coding_transcript_variant		2

Frequencies

GnomAD3 genomes AF: 0.598 AC: 90843 AN: 151900 Hom.: 27331 Cov.: 32

Gnomad AFR AF: 0.654

Gnomad AMI AF: 0.670

Gnomad AMR AF: 0.603

Gnomad ASJ AF: 0.610

Gnomad EAS AF: 0.618

Gnomad SAS AF: 0.532

Gnomad FIN AF: 0.617

Gnomad MID AF: 0.665

Gnomad NFE AF: 0.561

Gnomad OTH AF: 0.601

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

GnomAD4 genome AF: 0.598 AC: 90935 AN: 152018 Hom.: 27363 Cov.: 32 AF XY: 0.600 AC XY: 44600 AN XY: 74314

Gnomad4 AFR AF: 0.655

Gnomad4 AMR AF: 0.603

Gnomad4 ASJ AF: 0.610

Gnomad4 EAS AF: 0.619

Gnomad4 SAS AF: 0.531

Gnomad4 FIN AF: 0.617

Gnomad4 NFE AF: 0.561

Gnomad4 OTH AF: 0.598

Alfa AF: 0.570 Hom.: 12065

Bravo AF: 0.604

Asia WGS AF: 0.593 AC: 2064 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
Cadd	Benign	5.8
Dann	Benign	0.38

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: rs6931735; hg19: chr6-135624811;