chr10-59245484-G-T

Position:

• chr10-59245484-G-T

Variant summary

Our verdict is Likely benign. Variant got -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_032439.4(PHYHIPL):​c.1024G>T​(p.Val342Leu) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 14/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another nucleotide change resulting in the same amino acid substitution has been previously reported as Likely benign in UniProt.

• Frequency: Genomes: not found (cov: 32)
• Consequence: PHYHIPL NM_032439.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.58

Genes affected

PHYHIPL (HGNC:29378): (phytanoyl-CoA 2-hydroxylase interacting protein like) Located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Likely_benign. Variant got -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.0645349).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
PHYHIPL	NM_032439.4	c.1024G>T	p.Val342Leu	missense_variant	5/5	ENST00000373880.9	NP_115815.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
PHYHIPL	ENST00000373880.9	c.1024G>T	p.Val342Leu	missense_variant	5/5	1	NM_032439.4	ENSP00000362987.4
PHYHIPL	ENST00000373878.3	c.946G>T	p.Val316Leu	missense_variant	5/5	1		ENSP00000362985.3
PHYHIPL	ENST00000486074.2	n.*965G>T		non_coding_transcript_exon_variant	6/6	2		ENSP00000423634.1
PHYHIPL	ENST00000486074.2	n.*965G>T		3_prime_UTR_variant	6/6	2		ENSP00000423634.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 61

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.046
BayesDel_addAF	Benign	-0.35	T
BayesDel_noAF	Benign	-0.75
CADD	Benign	15
DANN	Benign	0.83
DEOGEN2	Benign	0.020	T;.
Eigen	Benign	-0.77
Eigen_PC	Benign	-0.45
FATHMM_MKL	Benign	0.66	D
LIST_S2	Benign	0.035	T;T
M_CAP	Benign	0.0045	T
MetaRNN	Benign	0.065	T;T
MetaSVM	Benign	-1.0	T
MutationAssessor	Benign	-1.6	N;.
PrimateAI	Uncertain	0.74	T
PROVEAN	Benign	0.63	N;N
REVEL	Benign	0.11
Sift	Benign	1.0	T;T
Sift4G	Benign	1.0	T;T
Polyphen		0.0	B;B
Vest4		0.033
MutPred		0.26		Gain of glycosylation at S341 (P = 0.1116);.;
MVP		0.13
MPC		0.50
ClinPred		0.10	T
GERP RS		5.6
Varity_R		0.035
gMVP		0.094

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

Publications

LitVar

Other links and lift over

dbSNP: rs2452505; hg19: chr10-61005244;