chr10-70567570-C-T

Variant names:

• chr10-70567570-C-T
• rs1556612
• NM_014431.3:c.*837C>T

Variant summary

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

The NM_014431.3(PALD1):​c.*837C>T variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.197 in 152,972 control chromosomes in the GnomAD database, including 3,629 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 0.20 (3606 hom., cov: 32)
  • Exomes 𝑓: 0.22 (23 hom.)
• Consequence: PALD1 NM_014431.3 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.40
• Publications: 4 publications found

Genes affected

PALD1 (HGNC:23530): (phosphatase domain containing paladin 1) Predicted to enable protein tyrosine phosphatase activity. Predicted to be involved in peptidyl-tyrosine dephosphorylation. Located in cytosol. [provided by Alliance of Genome Resources, Apr 2022]

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 (AMR) allele frequency at 95% confidence interval = 0.362 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_014431.3. 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
	PALD1	NM_014431.3	MANE Select	c.*837C>T		3_prime_UTR	Exon 20 of 20	NP_055246.2	Q9ULE6

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PALD1	ENST00000263563.7	TSL:1 MANE Select	c.*837C>T		3_prime_UTR	Exon 20 of 20	ENSP00000263563.5	Q9ULE6
	PALD1	ENST00000893833.1		c.*837C>T		3_prime_UTR	Exon 21 of 21	ENSP00000563892.1
	PALD1	ENST00000893834.1		c.*837C>T		3_prime_UTR	Exon 21 of 21	ENSP00000563893.1

Frequencies

GnomAD3 genomes AF: 0.197 AC: 30022 AN: 152084 Hom.: 3592 Cov.: 32

Gnomad AFR AF: 0.0859

Gnomad AMI AF: 0.242

Gnomad AMR AF: 0.369

Gnomad ASJ AF: 0.263

Gnomad EAS AF: 0.164

Gnomad SAS AF: 0.253

Gnomad FIN AF: 0.122

Gnomad MID AF: 0.244

Gnomad NFE AF: 0.232

Gnomad OTH AF: 0.237

GnomAD4 exome AF: 0.218 AC: 168 AN: 770 Hom.: 23 Cov.: 0 AF XY: 0.222 AC XY: 118 AN XY: 532

African (AFR) AF: 0.250 AC: 1 AN: 4

American (AMR) AF: 1.00 AC: 2 AN: 2

Ashkenazi Jewish (ASJ) AF: 0.333 AC: 2 AN: 6

East Asian (EAS) AF: 0.750 AC: 3 AN: 4

South Asian (SAS) AF: 0.250 AC: 1 AN: 4

European-Finnish (FIN) AF: 0.122 AC: 53 AN: 434

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 2

European-Non Finnish (NFE) AF: 0.333 AC: 100 AN: 300

Other (OTH) AF: 0.429 AC: 6 AN: 14

GnomAD4 genome AF: 0.197 AC: 30039 AN: 152202 Hom.: 3606 Cov.: 32 AF XY: 0.198 AC XY: 14756 AN XY: 74410

African (AFR) AF: 0.0858 AC: 3563 AN: 41542

American (AMR) AF: 0.370 AC: 5654 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.263 AC: 913 AN: 3472

East Asian (EAS) AF: 0.164 AC: 849 AN: 5170

South Asian (SAS) AF: 0.252 AC: 1219 AN: 4828

European-Finnish (FIN) AF: 0.122 AC: 1297 AN: 10602

Middle Eastern (MID) AF: 0.255 AC: 75 AN: 294

European-Non Finnish (NFE) AF: 0.232 AC: 15755 AN: 67976

Other (OTH) AF: 0.234 AC: 494 AN: 2114

Alfa AF: 0.219 Hom.: 618

Bravo AF: 0.215

Asia WGS AF: 0.227 AC: 788 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	2.1
DANN	Benign	0.69
PhyloP100		-1.4
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: rs1556612; hg19: chr10-72327326; COSMIC: COSV54971679;