NM_021930.6:c.375T>C

Variant names:

Variant summary

Our verdict is Benign. The variant received -21 ACMG points: 0P and 21B. BP4_StrongBP6_Very_StrongBP7BS1BS2

The NM_021930.6(RINT1):c.375T>C(p.Thr125Thr) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000857 in 1,614,140 control chromosomes in the GnomAD database, including 16 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).

Frequency

Genomes: 𝑓 0.0045 ( 8 hom., cov: 32)

Exomes 𝑓: 0.00048 ( 8 hom. )

Consequence

RINT1
NM_021930.6 synonymous

Scores

Clinical Significance

Benign/Likely benign criteria provided, multiple submitters, no conflicts B:4

Conservation

PhyloP100: -1.36

Publications

1 publications found

Variant links:

Genes affected

RINT1 (HGNC:21876): (RAD50 interactor 1) This gene encodes a protein first identified for its ability to interact with the RAD50 double strand break repair protein, with the resulting interaction implicated in the regulation of cell cycle progression and telomere length. The encoded protein may also play a role in trafficking of cellular cargo from the endosome to the trans-Golgi network. Mutations in this gene may be associated with breast cancer in human patients. [provided by RefSeq, Oct 2016]

RINT1 Gene-Disease associations (from GenCC):

infantile liver failure syndrome 3
Inheritance: AR Classification: STRONG, LIMITED Submitted by: Labcorp Genetics (formerly Invitae), G2P, Ambry Genetics
infantile liver failure syndrome 2
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet
breast cancer
Inheritance: AD Classification: NO_KNOWN Submitted by: Ambry Genetics
familial ovarian cancer
Inheritance: AD Classification: NO_KNOWN Submitted by: ClinGen
hereditary breast carcinoma
Inheritance: AD Classification: NO_KNOWN Submitted by: ClinGen

RINT1 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -21 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.9).

BP6

Variant 7-105542509-T-C is Benign according to our data. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-105542509-T-C is described in CliVar as Benign/Likely_benign. Clinvar id is 416387.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BP7

Synonymous conserved (PhyloP=-1.36 with no splicing effect.

BS1

Variant frequency is greater than expected in population afr. GnomAd4 allele frequency = 0.00452 (689/152298) while in subpopulation AFR AF = 0.0158 (656/41562). AF 95% confidence interval is 0.0148. There are 8 homozygotes in GnomAd4. There are 330 alleles in the male GnomAd4 subpopulation. Median coverage is 32. This position passed quality control check.

BS2

High Homozygotes in GnomAd4 at 8 AR,AD gene

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RINT1	NM_021930.6 link	c.375T>C	p.Thr125Thr	synonymous_variant	Exon 4 of 15	ENST00000257700.7	NP_068749.3	Q6NUQ1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
RINT1	ENST00000257700.7 link	c.375T>C	p.Thr125Thr	synonymous_variant	Exon 4 of 15	1	NM_021930.6	ENSP00000257700.2		Q6NUQ1

Frequencies

GnomAD3 genomes

AF:

0.00454

AC:

691

AN:

152180

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.0159

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.00170

Gnomad ASJ

AF:

0.00

Gnomad EAS

AF:

0.00

Gnomad SAS

AF:

0.000207

Gnomad FIN

AF:

0.00

Gnomad MID

AF:

0.00

Gnomad NFE

AF:

0.0000588

Gnomad OTH

AF:

0.00144

GnomAD2 exomes

AF:

0.00120

AC:

301

AN:

251424

AF XY:

0.000986

show subpopulations

Gnomad AFR exome

AF:

0.0166

Gnomad AMR exome

AF:

0.000665

Gnomad ASJ exome

AF:

0.00

Gnomad EAS exome

AF:

0.00

Gnomad FIN exome

AF:

0.00

Gnomad NFE exome

AF:

0.0000176

Gnomad OTH exome

AF:

0.000977

GnomAD4 exome

AF:

0.000475

AC:

695

AN:

1461842

Hom.:

Cov.:

AF XY:

0.000414

AC XY:

301

AN XY:

727220

show subpopulations

African (AFR)

AF:

0.0177

AC:

591

AN:

33478

American (AMR)

AF:

0.000738

AC:

AN:

44718

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

26136

East Asian (EAS)

AF:

0.00

AC:

AN:

39698

South Asian (SAS)

AF:

0.0000232

AC:

AN:

86244

European-Finnish (FIN)

AF:

0.00

AC:

AN:

53418

Middle Eastern (MID)

AF:

0.000347

AC:

AN:

5768

European-Non Finnish (NFE)

AF:

0.00000630

AC:

AN:

1111988

Other (OTH)

AF:

0.000993

AC:

AN:

60394

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.478

Heterozygous variant carriers

115

153

191

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Exome Hom

Variant carriers

100

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

AF:

0.00452

AC:

689

AN:

152298

Hom.:

Cov.:

AF XY:

0.00443

AC XY:

330

AN XY:

74482

show subpopulations

African (AFR)

AF:

0.0158

AC:

656

AN:

41562

American (AMR)

AF:

0.00170

AC:

AN:

15282

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

3472

East Asian (EAS)

AF:

0.00

AC:

AN:

5190

South Asian (SAS)

AF:

0.00

AC:

AN:

4828

European-Finnish (FIN)

AF:

0.00

AC:

AN:

10616

Middle Eastern (MID)

AF:

0.00

AC:

AN:

292

European-Non Finnish (NFE)

AF:

0.0000588

AC:

AN:

68032

Other (OTH)

AF:

0.00142

AC:

AN:

2112

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.498

Heterozygous variant carriers

129

161

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome Het

Genome Hom

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

Alfa

AF:

0.00221

Hom.:

Bravo

AF:

0.00514

Asia WGS

AF:

0.000289

AC:

AN:

3478

EpiCase

AF:

0.00

EpiControl

AF:

0.0000593

ClinVar

Significance: Benign/Likely benign

Submissions summary: Benign:4

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not provided

Benign:2

Breakthrough Genomics, Breakthrough Genomics

Significance:Benign

Review Status:criteria provided, single submitter

Collection Method:not provided

- -

Jan 19, 2025

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

not specified

Benign:1

Aug 13, 2020

Ambry Genetics

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. -

RINT1-related disorder

Benign:1

Jul 29, 2019

PreventionGenetics, part of Exact Sciences

Significance:Benign

Review Status:no assertion criteria provided

Collection Method:clinical testing

This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.90

CADD

Benign

2.4

(source)

DANN

Benign

0.51

PhyloP100

-1.4

Mutation Taster

=100/0

polymorphism

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.020

Details are displayed if max score is > 0.2

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

Publications

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over