rs1678199

chr2-230480845-C-Achr2-230480845-C-T

Variant summary

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

The NM_001080391.2(SP100):c.1600+6398C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.869 in 152,182 control chromosomes in the GnomAD database, including 58,065 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 0.87 (58065 hom., cov: 31)
• Consequence: SP100 NM_001080391.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.395

Genes affected

SP100 (HGNC:11206): (SP100 nuclear antigen) This gene encodes a subnuclear organelle and major component of the PML (promyelocytic leukemia)-SP100 nuclear bodies. PML and SP100 are covalently modified by the SUMO-1 modifier, which is considered crucial to nuclear body interactions. The encoded protein binds heterochromatin proteins and is thought to play a role in tumorigenesis, immunity, and gene regulation. Alternatively spliced variants have been identified for this gene; one of which encodes a high-mobility group protein. [provided by RefSeq, Aug 2011]

LOC101928816 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.95).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.958 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
SP100	NM_001080391.2	c.1600+6398C>A		intron_variant		ENST00000340126.9
LOC101928816	XR_427235.4	n.471+17791G>T		intron_variant, non_coding_transcript_variant
SP100	NM_001206701.2	c.1600+6398C>A		intron_variant
SP100	NM_003113.4	c.1600+6398C>A		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
SP100	ENST00000340126.9	c.1600+6398C>A		intron_variant		1	NM_001080391.2	P1

Frequencies

GnomAD3 genomes AF: 0.869 AC: 132115 AN: 152064 Hom.: 58010 Cov.: 31

Gnomad AFR AF: 0.966

Gnomad AMI AF: 0.779

Gnomad AMR AF: 0.761

Gnomad ASJ AF: 0.927

Gnomad EAS AF: 0.586

Gnomad SAS AF: 0.878

Gnomad FIN AF: 0.853

Gnomad MID AF: 0.934

Gnomad NFE AF: 0.855

Gnomad OTH AF: 0.872

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

GnomAD4 genome AF: 0.869 AC: 132221 AN: 152182 Hom.: 58065 Cov.: 31 AF XY: 0.864 AC XY: 64297 AN XY: 74396

Gnomad4 AFR AF: 0.966

Gnomad4 AMR AF: 0.760

Gnomad4 ASJ AF: 0.927

Gnomad4 EAS AF: 0.585

Gnomad4 SAS AF: 0.878

Gnomad4 FIN AF: 0.853

Gnomad4 NFE AF: 0.855

Gnomad4 OTH AF: 0.874

Alfa AF: 0.860 Hom.: 3426

Bravo AF: 0.862

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.95
Cadd	Benign	0.91
Dann	Benign	0.65

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: rs1678199; hg19: chr2-231345560;