rs4883198

Variant names:

• chr12-8917770-T-A
• rs4883198
• NM_004426.3:c.93T>A

Your query was ambiguous. Multiple possible variants found:

• chr12-8917770-T-A
• chr12-8917770-T-C
• chr12-8917770-T-G

Variant summary

Our verdict is Benign. The variant received -21 ACMG points: 0P and 21B. BP4_Strong BP6_Very_Strong BP7 BA1

The NM_004426.3(PHC1):​c.93T>A​(p.Leu31Leu) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.715 in 1,561,100 control chromosomes in the GnomAD database, including 401,041 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.68 (34995 hom., cov: 30)
  • Exomes 𝑓: 0.72 (366046 hom.)
• Consequence: PHC1 NM_004426.3 synonymous
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:3
• Conservation: PhyloP100: -0.0380
• Publications: 27 publications found

Genes affected

PHC1 (HGNC:3182): (polyhomeotic homolog 1) This gene is a homolog of the Drosophila polyhomeotic gene, which is a member of the Polycomb group of genes. The gene product is a component of a multimeric protein complex that contains EDR2 and the vertebrate Polycomb protein BMH1. The gene product, the EDR2 protein, and the Drosophila polyhomeotic protein share 2 highly conserved domains, named homology domains I and II. These domains are involved in protein-protein interactions and may mediate heterodimerization of the protein encoded by this gene and the EDR2 protein. [provided by RefSeq, Jul 2008]

PHC1 Gene-Disease associations (from GenCC):

• autosomal recessive primary microcephaly

  Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet
• microcephaly 11, primary, autosomal recessive

  Inheritance: AR Classification: LIMITED Submitted by: G2P, Labcorp Genetics (formerly Invitae)

ACMG classification

Our verdict: Benign. The variant received -21 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.5).
• BP6: Variant 12-8917770-T-A is Benign according to our data. Variant chr12-8917770-T-A is described in ClinVar as Benign. ClinVar VariationId is 1271948.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BP7: Synonymous conserved (PhyloP=-0.038 with no splicing effect.
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.811 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_004426.3. 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
	PHC1	NM_004426.3	MANE Select	c.93T>A	p.Leu31Leu	synonymous	Exon 2 of 15	NP_004417.2	P78364
	PHC1	NM_001413738.1		c.93T>A	p.Leu31Leu	synonymous	Exon 2 of 15	NP_001400667.1	P78364
	PHC1	NM_001413739.1		c.93T>A	p.Leu31Leu	synonymous	Exon 2 of 15	NP_001400668.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PHC1	ENST00000544916.6	TSL:1 MANE Select	c.93T>A	p.Leu31Leu	synonymous	Exon 2 of 15	ENSP00000437659.1	P78364
	PHC1	ENST00000543824.5	TSL:1	c.93T>A	p.Leu31Leu	synonymous	Exon 3 of 16	ENSP00000440674.1	P78364
	PHC1	ENST00000433083.6	TSL:1	c.93T>A	p.Leu31Leu	synonymous	Exon 2 of 14	ENSP00000399194.2	J3KQH6

Frequencies

GnomAD3 genomes AF: 0.675 AC: 102498 AN: 151758 Hom.: 34987 Cov.: 30

Gnomad AFR AF: 0.589

Gnomad AMI AF: 0.637

Gnomad AMR AF: 0.625

Gnomad ASJ AF: 0.804

Gnomad EAS AF: 0.752

Gnomad SAS AF: 0.833

Gnomad FIN AF: 0.685

Gnomad MID AF: 0.788

Gnomad NFE AF: 0.714

Gnomad OTH AF: 0.687

GnomAD2 exomes AF: 0.709 AC: 157941 AN: 222630 AF XY: 0.721

Gnomad AFR exome AF: 0.578

Gnomad AMR exome AF: 0.618

Gnomad ASJ exome AF: 0.800

Gnomad EAS exome AF: 0.743

Gnomad FIN exome AF: 0.688

Gnomad NFE exome AF: 0.712

Gnomad OTH exome AF: 0.730

GnomAD4 exome AF: 0.719 AC: 1012923 AN: 1409224 Hom.: 366046 Cov.: 25 AF XY: 0.723 AC XY: 507856 AN XY: 702106

African (AFR) AF: 0.583 AC: 17906 AN: 30722

American (AMR) AF: 0.621 AC: 24730 AN: 39814

Ashkenazi Jewish (ASJ) AF: 0.800 AC: 20292 AN: 25366

East Asian (EAS) AF: 0.745 AC: 27112 AN: 36376

South Asian (SAS) AF: 0.829 AC: 67275 AN: 81138

European-Finnish (FIN) AF: 0.683 AC: 36287 AN: 53094

Middle Eastern (MID) AF: 0.771 AC: 4393 AN: 5696

European-Non Finnish (NFE) AF: 0.716 AC: 772643 AN: 1078584

Other (OTH) AF: 0.724 AC: 42285 AN: 58434

GnomAD4 genome AF: 0.675 AC: 102545 AN: 151876 Hom.: 34995 Cov.: 30 AF XY: 0.674 AC XY: 49997 AN XY: 74222

African (AFR) AF: 0.589 AC: 24360 AN: 41386

American (AMR) AF: 0.625 AC: 9539 AN: 15270

Ashkenazi Jewish (ASJ) AF: 0.804 AC: 2787 AN: 3466

East Asian (EAS) AF: 0.753 AC: 3873 AN: 5142

South Asian (SAS) AF: 0.832 AC: 4014 AN: 4824

European-Finnish (FIN) AF: 0.685 AC: 7205 AN: 10522

Middle Eastern (MID) AF: 0.793 AC: 233 AN: 294

European-Non Finnish (NFE) AF: 0.714 AC: 48506 AN: 67950

Other (OTH) AF: 0.686 AC: 1448 AN: 2112

Alfa AF: 0.694 Hom.: 9677

Bravo AF: 0.665

Asia WGS AF: 0.763 AC: 2652 AN: 3478

ClinVar

ClinVar submissions

Significance: Benign

Revision: criteria provided, multiple submitters, no conflicts

Pathogenic	VUS	Benign	Condition
-	-	2	not provided (2)
-	-	1	Microcephaly 11, primary, autosomal recessive (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.50
CADD	Benign	4.4
DANN	Benign	0.68
PhyloP100		-0.038
PromoterAI		0.00060	Neutral
Mutation Taster		=295/5	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: rs4883198; hg19: chr12-9070366; COSMIC: COSV70417649; COSMIC: COSV70417649;