rs9437983

Variant names:

• chr1-147903563-A-G
• rs9437983
• NM_005267.5:c.-12+702A>G

Variant summary

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

The NM_005267.5(GJA8):​c.-12+702A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.3 in 152,096 control chromosomes in the GnomAD database, including 7,076 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 0.30 (7076 hom., cov: 32)
• Consequence: GJA8 NM_005267.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.162

Genes affected

GJA8 (HGNC:4281): (gap junction protein alpha 8) This gene encodes a transmembrane connexin protein that is necessary for lens growth and maturation of lens fiber cells. The encoded protein is a component of gap junction channels and functions in a calcium and pH-dependent manner. Mutations in this gene have been associated with zonular pulverulent cataracts, nuclear progressive cataracts, and cataract-microcornea syndrome. [provided by RefSeq, Dec 2009]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.393 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
GJA8	NM_005267.5	c.-12+702A>G		intron_variant	Intron 1 of 1	ENST00000369235.2	NP_005258.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
GJA8	ENST00000369235.2	c.-12+702A>G		intron_variant	Intron 1 of 1	6	NM_005267.5	ENSP00000358238.1

Frequencies

GnomAD3 genomes AF: 0.300 AC: 45546 AN: 151978 Hom.: 7060 Cov.: 32

Gnomad AFR AF: 0.250

Gnomad AMI AF: 0.282

Gnomad AMR AF: 0.402

Gnomad ASJ AF: 0.298

Gnomad EAS AF: 0.383

Gnomad SAS AF: 0.186

Gnomad FIN AF: 0.262

Gnomad MID AF: 0.245

Gnomad NFE AF: 0.314

Gnomad OTH AF: 0.330

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

GnomAD4 genome AF: 0.300 AC: 45598 AN: 152096 Hom.: 7076 Cov.: 32 AF XY: 0.299 AC XY: 22195 AN XY: 74352

Gnomad4 AFR AF: 0.250

Gnomad4 AMR AF: 0.402

Gnomad4 ASJ AF: 0.298

Gnomad4 EAS AF: 0.383

Gnomad4 SAS AF: 0.186

Gnomad4 FIN AF: 0.262

Gnomad4 NFE AF: 0.314

Gnomad4 OTH AF: 0.333

Alfa AF: 0.306 Hom.: 1428

Bravo AF: 0.312

Asia WGS AF: 0.292 AC: 1014 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	2.0
DANN	Benign	0.51

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs9437983; hg19: chr1-147375689;