6-150150458-T-G

Variant names:

• chr6-150150458-T-G
• rs1408504
• NM_030949.3:c.306+6960T>G

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+6960T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.574 in 151,900 control chromosomes in the GnomAD database, including 25,206 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 0.57 (25206 hom., cov: 31)
• Consequence: PPP1R14C NM_030949.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.909
• Publications: 4 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=-0.85).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.698 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_030949.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PPP1R14C	NM_030949.3	MANE Select	c.306+6960T>G		intron	N/A	NP_112211.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PPP1R14C	ENST00000361131.5	TSL:1 MANE Select	c.306+6960T>G		intron	N/A	ENSP00000355260.4

Frequencies

GnomAD3 genomes AF: 0.574 AC: 87188 AN: 151782 Hom.: 25203 Cov.: 31

Gnomad AFR AF: 0.529

Gnomad AMI AF: 0.621

Gnomad AMR AF: 0.538

Gnomad ASJ AF: 0.691

Gnomad EAS AF: 0.717

Gnomad SAS AF: 0.568

Gnomad FIN AF: 0.591

Gnomad MID AF: 0.677

Gnomad NFE AF: 0.590

Gnomad OTH AF: 0.584

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

GnomAD4 genome AF: 0.574 AC: 87229 AN: 151900 Hom.: 25206 Cov.: 31 AF XY: 0.575 AC XY: 42697 AN XY: 74226

African (AFR) AF: 0.528 AC: 21883 AN: 41412

American (AMR) AF: 0.538 AC: 8225 AN: 15274

Ashkenazi Jewish (ASJ) AF: 0.691 AC: 2399 AN: 3470

East Asian (EAS) AF: 0.717 AC: 3702 AN: 5160

South Asian (SAS) AF: 0.568 AC: 2732 AN: 4810

European-Finnish (FIN) AF: 0.591 AC: 6224 AN: 10536

Middle Eastern (MID) AF: 0.673 AC: 198 AN: 294

European-Non Finnish (NFE) AF: 0.590 AC: 40079 AN: 67932

Other (OTH) AF: 0.581 AC: 1222 AN: 2102

Alfa AF: 0.592 Hom.: 32488

Bravo AF: 0.568

Asia WGS AF: 0.582 AC: 2025 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	1.1
DANN	Benign	0.74
PhyloP100		-0.91
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: rs1408504; hg19: chr6-150471594;