rs770512804

Variant names:

• chr10-101008490-C-A
• NM_001195263.2:c.3079G>T

Your query was ambiguous. Multiple possible variants found:

• chr10-101008490-C-A
• chr10-101008490-C-T

Variant summary

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

The NM_001195263.2(PDZD7):​c.3079G>T​(p.Ala1027Ser) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000073 in 1,368,992 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 9/12 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: not found (cov: 30)
  • Exomes 𝑓: 7.3e-7 (0 hom.)
• Consequence: PDZD7 NM_001195263.2 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.87

Genes affected

PDZD7 (HGNC:26257): (PDZ domain containing 7) This gene encodes a ciliary protein homologous to proteins which are mutated in Usher syndrome patients, and mutations and translocations involving this gene have been associated with two types of Usher syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2010]

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=0.058096945).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PDZD7	NM_001195263.2	c.3079G>T	p.Ala1027Ser	missense_variant	Exon 17 of 17	ENST00000619208.6	NP_001182192.1
PDZD7	XM_011540177.4	c.3079G>T	p.Ala1027Ser	missense_variant	Exon 18 of 18		XP_011538479.1
PDZD7	XM_047425767.1	c.3079G>T	p.Ala1027Ser	missense_variant	Exon 17 of 17		XP_047281723.1
PDZD7	XM_011540178.4	c.3076G>T	p.Ala1026Ser	missense_variant	Exon 17 of 17		XP_011538480.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PDZD7	ENST00000619208.6	c.3079G>T	p.Ala1027Ser	missense_variant	Exon 17 of 17	5	NM_001195263.2	ENSP00000480489.1
PDZD7	ENST00000474125.7	n.*3026G>T		non_coding_transcript_exon_variant	Exon 13 of 13	2		ENSP00000474447.1
PDZD7	ENST00000474125.7	n.*3026G>T		3_prime_UTR_variant	Exon 13 of 13	2		ENSP00000474447.1

Frequencies

GnomAD3 genomes Cov.: 30

GnomAD4 exome AF: 7.30e-7 AC: 1 AN: 1368992 Hom.: 0 Cov.: 32 AF XY: 0.00000148 AC XY: 1 AN XY: 674018

Gnomad4 AFR exome AF: 0.00

Gnomad4 AMR exome AF: 0.00

Gnomad4 ASJ exome AF: 0.00

Gnomad4 EAS exome AF: 0.00

Gnomad4 SAS exome AF: 0.00

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 9.35e-7

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome Cov.: 30

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.071
BayesDel_addAF	Benign	-0.22	T
BayesDel_noAF	Benign	-0.55
CADD	Benign	0.0080
DANN	Benign	0.44
Eigen	Benign	-1.8
Eigen_PC	Benign	-1.9
FATHMM_MKL	Benign	0.051	N
LIST_S2	Benign	0.23	.;T
MetaRNN	Benign	0.058	T;T
MetaSVM	Benign	-0.98	T
PrimateAI	Benign	0.27	T
Sift4G	Benign	1.0	.;T
Vest4		0.10
MVP		0.068
ClinPred		0.20	T
GERP RS		-7.1
Varity_R		0.051
gMVP		0.11

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr10-102768247;