12-110647784-C-T

Variant names:

• chr12-110647784-C-T
• rs200067409
• NM_001082538.3:c.1671C>T

Variant summary

Our verdict is Likely benign. Variant got -3 ACMG points: 2P and 5B. PM2 BP4_Moderate BP6_Moderate BP7

The NM_001082538.3(TCTN1):​c.1671C>T​(p.Ser557Ser) variant causes a synonymous 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. Variant has been reported in ClinVar as Likely benign (★). Synonymous variant affecting the same amino acid position (i.e. S557S) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: TCTN1 NM_001082538.3 synonymous
• Clinical Significance: Likely benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 0.457

Genes affected

TCTN1 (HGNC:26113): (tectonic family member 1) This gene encodes a member of a family of secreted and transmembrane proteins. The orthologous gene in mouse functions downstream of smoothened and rab23 to modulate hedgehog signal transduction. This protein is a component of the tectonic-like complex, which forms a barrier between the ciliary axoneme and the basal body. A mutation in this gene was found in a family with Joubert syndrome-13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]

HVCN1 (HGNC:28240): (hydrogen voltage gated channel 1) This gene encodes a voltage-gated protein channel protein expressed more highly in certain cells of the immune system. Phagocytic cells produce superoxide anions which require this channel protein, and in B cells this same process facilitates antibody production. This same channel protein, however, can also regulate functions in other cells including spermatozoa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]

ACMG classification

Verdict is Likely_benign. Variant got -3 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.16141188).
• BP6: Variant 12-110647784-C-T is Benign according to our data. Variant chr12-110647784-C-T is described in ClinVar as [Likely_benign]. Clinvar id is 1536019.Status of the report is criteria_provided_single_submitter, 1 stars.
• BP7: Synonymous conserved (PhyloP=0.457 with no splicing effect.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TCTN1	NM_001082538.3	c.1671C>T	p.Ser557Ser	synonymous_variant	Exon 14 of 15	ENST00000397659.9	NP_001076007.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TCTN1	ENST00000397659.9	c.1671C>T	p.Ser557Ser	synonymous_variant	Exon 14 of 15	1	NM_001082538.3	ENSP00000380779.4
TCTN1	ENST00000551590.5	c.1656C>T	p.Ser552Ser	synonymous_variant	Exon 14 of 15	1		ENSP00000448735.1
TCTN1	ENST00000397655.7	c.1614C>T	p.Ser538Ser	synonymous_variant	Exon 14 of 15	1		ENSP00000380775.3
TCTN1	ENST00000397656.8	n.*1289C>T		non_coding_transcript_exon_variant	Exon 15 of 16	2		ENSP00000380776.4
TCTN1	ENST00000480648.5	n.*932C>T		non_coding_transcript_exon_variant	Exon 15 of 16	5		ENSP00000437196.1
TCTN1	ENST00000495659.6	n.*1414C>T		non_coding_transcript_exon_variant	Exon 14 of 15	2		ENSP00000436673.2
TCTN1	ENST00000397656.8	n.*1289C>T		3_prime_UTR_variant	Exon 15 of 16	2		ENSP00000380776.4
TCTN1	ENST00000480648.5	n.*932C>T		3_prime_UTR_variant	Exon 15 of 16	5		ENSP00000437196.1
TCTN1	ENST00000495659.6	n.*1414C>T		3_prime_UTR_variant	Exon 14 of 15	2		ENSP00000436673.2

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD3 exomes AF: 0.00000401 AC: 1 AN: 249576 Hom.: 0 AF XY: 0.00000739 AC XY: 1 AN XY: 135408

Gnomad AFR exome AF: 0.0000646

Gnomad AMR exome AF: 0.00

Gnomad ASJ exome AF: 0.00

Gnomad EAS exome AF: 0.00

Gnomad SAS exome AF: 0.00

Gnomad FIN exome AF: 0.00

Gnomad NFE exome AF: 0.00

Gnomad OTH exome AF: 0.00

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ExAC AF: 0.00000827 AC: 1

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

Meckel-Gruber syndrome;C0431399:Joubert syndrome Benign:1

Jul 05, 2021

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Likely benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_addAF	Benign	-0.41	T
BayesDel_noAF	Benign	-0.65
CADD	Benign	10
DANN	Benign	0.73
Eigen	Benign	-0.56
Eigen_PC	Benign	-0.56
FATHMM_MKL	Benign	0.44	N
MetaRNN	Benign	0.16	T
MetaSVM	Benign	-0.73	T
PROVEAN	Pathogenic	-10	D
REVEL	Benign	0.16
MVP		0.23
ClinPred		0.19	T
GERP RS		1.5

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: rs200067409; hg19: chr12-111085589;