rs10421916

chr19-17818178-A-Gchr19-17818178-A-T

Variant summary

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

The NM_005543.4(INSL3):c.191-1119T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.69 in 151,878 control chromosomes in the GnomAD database, including 36,574 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 (36574 hom., cov: 30)
• Consequence: INSL3 NM_005543.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.41

Genes affected

INSL3 (HGNC:6086): (insulin like 3) This gene encodes a member of the insulin-like hormone superfamily. The encoded protein is mainly produced in gonadal tissues. Studies of the mouse counterpart suggest that this gene may be involved in the development of urogenital tract and female fertility. This protein may also act as a hormone to regulate growth and differentiation of gubernaculum, and thus mediating intra-abdominal testicular descent. Mutations in this gene may lead to cryptorchidism. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2012]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.784 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
INSL3	NM_005543.4	c.191-1119T>C		intron_variant		ENST00000317306.8
INSL3	NM_001265587.2	c.286-1119T>C		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
INSL3	ENST00000317306.8	c.191-1119T>C		intron_variant		1	NM_005543.4	P1
INSL3	ENST00000379695.5	c.286-1119T>C		intron_variant		1
INSL3	ENST00000598577.1	c.190-1097T>C		intron_variant		1

Frequencies

GnomAD3 genomes AF: 0.690 AC: 104768 AN: 151760 Hom.: 36527 Cov.: 30

Gnomad AFR AF: 0.791

Gnomad AMI AF: 0.639

Gnomad AMR AF: 0.636

Gnomad ASJ AF: 0.602

Gnomad EAS AF: 0.630

Gnomad SAS AF: 0.633

Gnomad FIN AF: 0.728

Gnomad MID AF: 0.608

Gnomad NFE AF: 0.651

Gnomad OTH AF: 0.651

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

GnomAD4 genome AF: 0.690 AC: 104864 AN: 151878 Hom.: 36574 Cov.: 30 AF XY: 0.692 AC XY: 51338 AN XY: 74222

Gnomad4 AFR AF: 0.791

Gnomad4 AMR AF: 0.636

Gnomad4 ASJ AF: 0.602

Gnomad4 EAS AF: 0.629

Gnomad4 SAS AF: 0.634

Gnomad4 FIN AF: 0.728

Gnomad4 NFE AF: 0.651

Gnomad4 OTH AF: 0.647

Alfa AF: 0.668 Hom.: 11195

Bravo AF: 0.687

Asia WGS AF: 0.610 AC: 2123 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
Cadd	Benign	1.0
Dann	Benign	0.68

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: rs10421916; hg19: chr19-17928987;