rs10499200

chr6-138450815-A-G

Variant summary

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

The NM_001144060.2(NHSL1):c.340-3622T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.131 in 152,170 control chromosomes in the GnomAD database, including 1,335 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 0.13 (1335 hom., cov: 32)
• Consequence: NHSL1 NM_001144060.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 2.01

Genes affected

NHSL1 (HGNC:21021): (NHS like 1) Predicted to be involved in cell differentiation. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.149 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
NHSL1	NM_001144060.2	c.340-3622T>C		intron_variant		ENST00000343505.10

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
NHSL1	ENST00000343505.10	c.340-3622T>C		intron_variant		5	NM_001144060.2	P3

Frequencies

GnomAD3 genomes AF: 0.131 AC: 19913 AN: 152052 Hom.: 1332 Cov.: 32

Gnomad AFR AF: 0.136

Gnomad AMI AF: 0.140

Gnomad AMR AF: 0.125

Gnomad ASJ AF: 0.136

Gnomad EAS AF: 0.00193

Gnomad SAS AF: 0.0827

Gnomad FIN AF: 0.0666

Gnomad MID AF: 0.165

Gnomad NFE AF: 0.151

Gnomad OTH AF: 0.150

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

GnomAD4 genome AF: 0.131 AC: 19933 AN: 152170 Hom.: 1335 Cov.: 32 AF XY: 0.124 AC XY: 9239 AN XY: 74406

Gnomad4 AFR AF: 0.137

Gnomad4 AMR AF: 0.125

Gnomad4 ASJ AF: 0.136

Gnomad4 EAS AF: 0.00193

Gnomad4 SAS AF: 0.0827

Gnomad4 FIN AF: 0.0666

Gnomad4 NFE AF: 0.151

Gnomad4 OTH AF: 0.149

Alfa AF: 0.149 Hom.: 3514

Bravo AF: 0.136

Asia WGS AF: 0.0580 AC: 202 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
Cadd	Benign	7.7
Dann	Benign	0.63

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: rs10499200; hg19: chr6-138771952;