NM_001363830.2:c.86+5786A>C

Variant names:

• chr17-35516493-T-G
• rs8070473
• NM_001363830.2:c.86+5786A>C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001363830.2(SLFN12L):​c.86+5786A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.716 in 152,186 control chromosomes in the GnomAD database, including 39,668 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 0.72 (39668 hom., cov: 33)
• Consequence: SLFN12L NM_001363830.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.318
• Publications: 9 publications found

Genes affected

SLFN12L (HGNC:33920): (schlafen family member 12 like) Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.02).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.775 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001363830.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SLFN12L	NM_001363830.2	MANE Select	c.86+5786A>C		intron	N/A	NP_001350759.2
	SLFN12L	NM_001195790.3		c.-288+5786A>C		intron	N/A	NP_001182719.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SLFN12L	ENST00000628453.4	TSL:5 MANE Select	c.86+5786A>C		intron	N/A	ENSP00000487397.4
	SLFN12L	ENST00000714259.1		n.803-1172A>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.716 AC: 108918 AN: 152068 Hom.: 39662 Cov.: 33

Gnomad AFR AF: 0.596

Gnomad AMI AF: 0.897

Gnomad AMR AF: 0.787

Gnomad ASJ AF: 0.675

Gnomad EAS AF: 0.571

Gnomad SAS AF: 0.680

Gnomad FIN AF: 0.805

Gnomad MID AF: 0.642

Gnomad NFE AF: 0.773

Gnomad OTH AF: 0.724

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

GnomAD4 genome AF: 0.716 AC: 108974 AN: 152186 Hom.: 39668 Cov.: 33 AF XY: 0.716 AC XY: 53259 AN XY: 74388

African (AFR) AF: 0.596 AC: 24715 AN: 41498

American (AMR) AF: 0.787 AC: 12040 AN: 15300

Ashkenazi Jewish (ASJ) AF: 0.675 AC: 2343 AN: 3470

East Asian (EAS) AF: 0.570 AC: 2952 AN: 5178

South Asian (SAS) AF: 0.681 AC: 3285 AN: 4826

European-Finnish (FIN) AF: 0.805 AC: 8523 AN: 10586

Middle Eastern (MID) AF: 0.643 AC: 189 AN: 294

European-Non Finnish (NFE) AF: 0.773 AC: 52576 AN: 68008

Other (OTH) AF: 0.725 AC: 1533 AN: 2114

Alfa AF: 0.748 Hom.: 134422

Bravo AF: 0.709

Asia WGS AF: 0.649 AC: 2253 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.39
DANN	Benign	0.56
PhyloP100		-0.32
Mutation Taster		=100/0	polymorphism (auto)

Splicing

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

Other links and lift over

dbSNP: rs8070473; hg19: chr17-33843512;