chr9-92094213-C-T

Position:

• chr9-92094213-C-T

Variant summary

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

The NM_006415.4(SPTLC1):​c.261-13250G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.531 in 152,066 control chromosomes in the GnomAD database, including 24,683 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 0.53 (24683 hom., cov: 32)
• Consequence: SPTLC1 NM_006415.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.08

Genes affected

SPTLC1 (HGNC:11277): (serine palmitoyltransferase long chain base subunit 1) This gene encodes a member of the class-II pyridoxal-phosphate-dependent aminotransferase family. The encoded protein is the long chain base subunit 1 of serine palmitoyltransferase. Serine palmitoyltransferase converts L-serine and palmitoyl-CoA to 3-oxosphinganine with pyridoxal 5'-phosphate and is the key enzyme in sphingolipid biosynthesis. Mutations in this gene were identified in patients with hereditary sensory neuropathy type 1. Alternatively spliced variants encoding different isoforms have been identified. Pseudogenes of this gene have been defined on chromosomes 1, 6, 10, and 13. [provided by RefSeq, Jul 2013]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.99).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.84 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SPTLC1	NM_006415.4	c.261-13250G>A		intron_variant		ENST00000262554.7	NP_006406.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SPTLC1	ENST00000262554.7	c.261-13250G>A		intron_variant		1	NM_006415.4	ENSP00000262554	P1

Frequencies

GnomAD3 genomes AF: 0.531 AC: 80683 AN: 151948 Hom.: 24633 Cov.: 32

Gnomad AFR AF: 0.847

Gnomad AMI AF: 0.372

Gnomad AMR AF: 0.569

Gnomad ASJ AF: 0.514

Gnomad EAS AF: 0.433

Gnomad SAS AF: 0.453

Gnomad FIN AF: 0.371

Gnomad MID AF: 0.541

Gnomad NFE AF: 0.372

Gnomad OTH AF: 0.493

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

GnomAD4 genome AF: 0.531 AC: 80792 AN: 152066 Hom.: 24683 Cov.: 32 AF XY: 0.532 AC XY: 39508 AN XY: 74320

Gnomad4 AFR AF: 0.847

Gnomad4 AMR AF: 0.569

Gnomad4 ASJ AF: 0.514

Gnomad4 EAS AF: 0.433

Gnomad4 SAS AF: 0.452

Gnomad4 FIN AF: 0.371

Gnomad4 NFE AF: 0.372

Gnomad4 OTH AF: 0.495

Alfa AF: 0.475 Hom.: 2170

Bravo AF: 0.559

Asia WGS AF: 0.489 AC: 1703 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.99
CADD	Benign	1.1
DANN	Benign	0.69

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: rs2895201; hg19: chr9-94856495; COSMIC: COSV52764580;