rs12332856

Variant names:

• chr6-150151352-G-A
• rs12332856
• NM_030949.3:c.306+7854G>A

Your query was ambiguous. Multiple possible variants found:

• chr6-150151352-G-A
• chr6-150151352-G-T

Variant summary

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

The NM_030949.3(PPP1R14C):​c.306+7854G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.176 in 152,122 control chromosomes in the GnomAD database, including 2,847 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 0.18 (2847 hom., cov: 31)
• Consequence: PPP1R14C NM_030949.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.626
• Publications: 3 publications found

Genes affected

PPP1R14C (HGNC:14952): (protein phosphatase 1 regulatory inhibitor subunit 14C) The degree of protein phosphorylation is regulated by a balance of protein kinase and phosphatase activities. Protein phosphatase-1 (PP1; see MIM 176875) is a signal-transducing phosphatase that influences neuronal activity, protein synthesis, metabolism, muscle contraction, and cell division. PPP1R14C is an inhibitor of PP1 (Liu et al., 2002 [PubMed 11812771]).[supplied by OMIM, Feb 2010]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.8).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.28 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PPP1R14C	NM_030949.3	c.306+7854G>A		intron_variant	Intron 1 of 3	ENST00000361131.5	NP_112211.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PPP1R14C	ENST00000361131.5	c.306+7854G>A		intron_variant	Intron 1 of 3	1	NM_030949.3	ENSP00000355260.4

Frequencies

GnomAD3 genomes AF: 0.176 AC: 26785 AN: 152004 Hom.: 2850 Cov.: 31

Gnomad AFR AF: 0.0734

Gnomad AMI AF: 0.285

Gnomad AMR AF: 0.255

Gnomad ASJ AF: 0.142

Gnomad EAS AF: 0.0309

Gnomad SAS AF: 0.294

Gnomad FIN AF: 0.244

Gnomad MID AF: 0.101

Gnomad NFE AF: 0.214

Gnomad OTH AF: 0.167

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

GnomAD4 genome AF: 0.176 AC: 26792 AN: 152122 Hom.: 2847 Cov.: 31 AF XY: 0.180 AC XY: 13374 AN XY: 74346

African (AFR) AF: 0.0731 AC: 3037 AN: 41526

American (AMR) AF: 0.255 AC: 3894 AN: 15278

Ashkenazi Jewish (ASJ) AF: 0.142 AC: 493 AN: 3468

East Asian (EAS) AF: 0.0308 AC: 159 AN: 5170

South Asian (SAS) AF: 0.293 AC: 1408 AN: 4802

European-Finnish (FIN) AF: 0.244 AC: 2582 AN: 10586

Middle Eastern (MID) AF: 0.102 AC: 30 AN: 294

European-Non Finnish (NFE) AF: 0.214 AC: 14575 AN: 67978

Other (OTH) AF: 0.168 AC: 354 AN: 2108

Alfa AF: 0.144 Hom.: 472

Bravo AF: 0.174

Asia WGS AF: 0.166 AC: 574 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.80
CADD	Benign	3.8
DANN	Benign	0.72
PhyloP100		-0.63
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: rs12332856; hg19: chr6-150472488;