rs2031633

Variant names:

• chr13-46022005-C-G
• rs2031633
• NM_001330564.2:c.340-1448G>C

Your query was ambiguous. Multiple possible variants found:

• chr13-46022005-C-G
• chr13-46022005-C-T

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001330564.2(ZC3H13):​c.340-1448G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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)
• Consequence: ZC3H13 NM_001330564.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.328
• Publications: 3 publications found

Genes affected

ZC3H13 (HGNC:20368): (zinc finger CCCH-type containing 13) Enables RNA binding activity. Involved in mRNA methylation. Located in nuclear speck. Part of RNA N6-methyladenosine methyltransferase complex. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001330564.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ZC3H13	NM_001330564.2	MANE Select	c.340-1448G>C		intron	N/A	NP_001317493.1	A0A7I2V4I5
	ZC3H13	NM_001382211.1		c.340-1448G>C		intron	N/A	NP_001369140.1
	ZC3H13	NM_001382212.1		c.340-1448G>C		intron	N/A	NP_001369141.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ZC3H13	ENST00000679008.1	MANE Select	c.340-1448G>C		intron	N/A	ENSP00000503994.1	A0A7I2V4I5
	ZC3H13	ENST00000282007.7	TSL:1	c.340-1448G>C		intron	N/A	ENSP00000282007.3	Q5T200-2
	ZC3H13	ENST00000929097.1		c.340-1448G>C		intron	N/A	ENSP00000599156.1

Frequencies

GnomAD3 genomes Cov.: 31

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

GnomAD4 genome Cov.: 31

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	3.1
DANN	Benign	0.56
PhyloP100		0.33

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

Other links and lift over

dbSNP: rs2031633; hg19: chr13-46596140;