rs1363222776

Variant names:

• chr19-9324706-C-A
• NM_032497.3:c.-194C>A

Your query was ambiguous. Multiple possible variants found:

• chr19-9324706-C-A
• chr19-9324706-C-G
• chr19-9324706-C-T

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_032497.3(ZNF559):​c.-194C>A variant causes a 5 prime UTR premature start codon gain change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000000724 in 1,381,642 control chromosomes in the GnomAD database, with no homozygous occurrence. 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: not found (cov: 31)
  • Exomes 𝑓: 7.2e-7 (0 hom.)
• Consequence: ZNF559 NM_032497.3 5_prime_UTR_premature_start_codon_gain
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.943

Genes affected

ZNF559 (HGNC:28197): (zinc finger protein 559) Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

ZNF559-ZNF177 (HGNC:42964): (ZNF559-ZNF177 readthrough) This locus represents naturally occurring read-through transcription between the neighboring zinc finger protein 559 (ZNF559) and zinc finger protein 177 (ZNF177) genes on chromosome 19. Alternative splicing results in multiple transcript variants, which encode the ZNF177 protein due to either leaky scanning by ribosomes, or absence of the ZNF559 start codon. [provided by RefSeq, Jan 2011]

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.08611882).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ZNF559	NM_032497.3	c.-194C>A		5_prime_UTR_premature_start_codon_gain_variant	Exon 2 of 7	ENST00000603380.6	NP_115886.1
ZNF559	NM_032497.3	c.-194C>A		5_prime_UTR_variant	Exon 2 of 7	ENST00000603380.6	NP_115886.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ZNF559	ENST00000603380	c.-194C>A		5_prime_UTR_premature_start_codon_gain_variant	Exon 2 of 7	2	NM_032497.3	ENSP00000474760.1
ZNF559-ZNF177	ENST00000541595	c.-554C>A		5_prime_UTR_premature_start_codon_gain_variant	Exon 2 of 12	2		ENSP00000445323.1
ZNF559	ENST00000603380	c.-194C>A		5_prime_UTR_variant	Exon 2 of 7	2	NM_032497.3	ENSP00000474760.1
ZNF559-ZNF177	ENST00000541595	c.-554C>A		5_prime_UTR_variant	Exon 2 of 12	2		ENSP00000445323.1

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome AF: 7.24e-7 AC: 1 AN: 1381642 Hom.: 0 Cov.: 33 AF XY: 0.00 AC XY: 0 AN XY: 681804

Gnomad4 AFR exome AF: 0.00

Gnomad4 AMR exome AF: 0.00

Gnomad4 ASJ exome AF: 0.00

Gnomad4 EAS exome AF: 0.00

Gnomad4 SAS exome AF: 0.00

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 9.28e-7

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome Cov.: 31

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_addAF	Benign	-0.27	T
BayesDel_noAF	Benign	-0.63
CADD	Benign	4.7
DANN	Benign	0.25
FATHMM_MKL	Benign	0.013	N
LIST_S2	Benign	0.42	T;T
M_CAP	Benign	0.00091	T
MetaRNN	Benign	0.086	T;T
PrimateAI	Benign	0.45	T
Sift4G	Uncertain	0.012	D;T
Vest4		0.24
MVP		0.20
GERP RS		-0.20
gMVP		0.50

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.020		Details are displayed if max score is > 0.2

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

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr19-9435382;