NM_001105564.2:c.801+147C>G

Variant names:

• chr6-31154349-G-C
• rs2073717
• NM_001105564.2:c.801+147C>G

Variant summary

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

The NM_001105564.2(CCHCR1):​c.801+147C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.602 in 679,004 control chromosomes in the GnomAD database, including 124,242 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 0.60 (27563 hom., cov: 32)
  • Exomes 𝑓: 0.60 (96679 hom.)
• Consequence: CCHCR1 NM_001105564.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0410
• Publications: 17 publications found

Genes affected

CCHCR1 (HGNC:13930): (coiled-coil alpha-helical rod protein 1) This gene encodes a protein with five coiled-coil alpha-helical rod domains that is thought to act as a regulator of mRNA metabolism through its interaction with mRNA-decapping protein 4. It localizes to P-bodies, the site of mRNA metabolism, with an N-terminus that is required for this subcellular localization, suggesting it is a P-body component. Naturally occurring mutations in this gene are associated with psoriasis. [provided by RefSeq, May 2017]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.642 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001105564.2. 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
	CCHCR1	NM_001105564.2	MANE Select	c.801+147C>G		intron	N/A	NP_001099034.1	Q8TD31-2
	CCHCR1	NM_001394641.1		c.828+147C>G		intron	N/A	NP_001381570.1
	CCHCR1	NM_001105563.3		c.693+147C>G		intron	N/A	NP_001099033.1	Q8TD31-3

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CCHCR1	ENST00000396268.8	TSL:1 MANE Select	c.801+147C>G		intron	N/A	ENSP00000379566.3	Q8TD31-2
	CCHCR1	ENST00000451521.6	TSL:1	c.693+147C>G		intron	N/A	ENSP00000401039.2	Q8TD31-3
	CCHCR1	ENST00000376266.9	TSL:1	c.534+147C>G		intron	N/A	ENSP00000365442.5	Q8TD31-1

Frequencies

GnomAD3 genomes AF: 0.601 AC: 91401 AN: 151960 Hom.: 27563 Cov.: 32

Gnomad AFR AF: 0.580

Gnomad AMI AF: 0.671

Gnomad AMR AF: 0.652

Gnomad ASJ AF: 0.769

Gnomad EAS AF: 0.606

Gnomad SAS AF: 0.617

Gnomad FIN AF: 0.635

Gnomad MID AF: 0.741

Gnomad NFE AF: 0.586

Gnomad OTH AF: 0.623

GnomAD4 exome AF: 0.603 AC: 317554 AN: 526928 Hom.: 96679 AF XY: 0.603 AC XY: 167408 AN XY: 277468

African (AFR) AF: 0.580 AC: 8368 AN: 14424

American (AMR) AF: 0.659 AC: 16076 AN: 24408

Ashkenazi Jewish (ASJ) AF: 0.761 AC: 11104 AN: 14590

East Asian (EAS) AF: 0.601 AC: 20157 AN: 33564

South Asian (SAS) AF: 0.632 AC: 28566 AN: 45196

European-Finnish (FIN) AF: 0.626 AC: 23214 AN: 37062

Middle Eastern (MID) AF: 0.673 AC: 2470 AN: 3668

European-Non Finnish (NFE) AF: 0.584 AC: 189928 AN: 325240

Other (OTH) AF: 0.614 AC: 17671 AN: 28776

GnomAD4 genome AF: 0.601 AC: 91436 AN: 152076 Hom.: 27563 Cov.: 32 AF XY: 0.605 AC XY: 44999 AN XY: 74348

African (AFR) AF: 0.580 AC: 24043 AN: 41484

American (AMR) AF: 0.652 AC: 9974 AN: 15292

Ashkenazi Jewish (ASJ) AF: 0.769 AC: 2671 AN: 3472

East Asian (EAS) AF: 0.606 AC: 3130 AN: 5162

South Asian (SAS) AF: 0.615 AC: 2958 AN: 4812

European-Finnish (FIN) AF: 0.635 AC: 6708 AN: 10566

Middle Eastern (MID) AF: 0.731 AC: 215 AN: 294

European-Non Finnish (NFE) AF: 0.586 AC: 39808 AN: 67972

Other (OTH) AF: 0.624 AC: 1320 AN: 2114

Alfa AF: 0.603 Hom.: 15267

Bravo AF: 0.606

Asia WGS AF: 0.648 AC: 2252 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	3.8
DANN	Benign	0.55
PhyloP100		-0.041
Mutation Taster		=100/0	polymorphism (auto)

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: rs2073717; hg19: chr6-31122126;