NM_000214.3:c.388-11_388-8delTTGT

Variant names:

• chr20-10664021-GACAA-G
• rs750004416
• NM_000214.3:c.388-11_388-8delTTGT

GermlineCancer (beta)

Variant summary

Our verdict is Likely benign.

-2 Likely Benign

-7

-6

-1

0

+5

+6

+9

+10

BenignB

Likely BenignLB

UncertainVUS

Likely PathogenicLP

PathogenicP

The variant received -2 classification points (ACMG Germline Pathogenicity v2019). BP6_Moderate

The NM_000214.3(JAG1):c.388-11_388-8delTTGT variant causes a splice region, intron change. Note: allele frequency estimates from gnomAD may be inaccurate for this variant type (MNP or indel longer than 3 bp) due to technology limitations. The variant allele was found at a cumulative frequency of 0.0000263 (AC=4) in the gnomAD database across 152,288 control chromosomes (no homozygotes observed). The grpmax filtering allele frequency (95% CI) is 0.000173. Note: a gnomAD entry for this variant shows a statistical allele-bias signature, consistent with mosaic/somatic contamination (e.g. age-related clonal hematopoiesis) rather than true inherited population frequency — this frequency should not be read as evidence of a common, benign germline variant. Splicing prediction tools (SpliceAI) predict no significant impact on normal splicing. The affected nucleotide is highly conserved across species (PhyloP 100-way vertebrate score: 8.57). Variant has been reported in ClinVar as Benign/Likely Benign (★).

• Frequency:
  • Genomes: 𝑓 0.000026 (0 hom., cov: 32)
  • Exomes 𝑓: 0.000023 (0 hom.)
• Consequence: JAG1 NM_000214.3 splice_region, intron
• Clinical Significance: Likely benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 8.57
• Publications: 0 publications found

Genes affected

JAG1 (HGNC:6188): (jagged canonical Notch ligand 1) The jagged 1 protein encoded by JAG1 is the human homolog of the Drosophilia jagged protein. Human jagged 1 is the ligand for the receptor notch 1, the latter is involved in signaling processes. Mutations that alter the jagged 1 protein cause Alagille syndrome. Jagged 1 signalling through notch 1 has also been shown to play a role in hematopoiesis. [provided by RefSeq, Nov 2019]

JAG1 Gene-Disease associations (from GenCC):

• Alagille syndrome due to a JAG1 point mutation

  Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: PanelApp Australia, Labcorp Genetics (formerly Invitae), Ambry Genetics, G2P
• Charcot-Marie-Tooth disease, axonal, Type 2HH

  Inheritance: AD Classification: STRONG, LIMITED Submitted by: Labcorp Genetics (formerly Invitae), Ambry Genetics, PanelApp Australia
• tetralogy of fallot

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet

Classification according to ACMG Germline Pathogenicity v2019

Classification was made for transcript:

Our verdict: Likely_benign. The variant received -2 points.

Apply	Criterion Code & Title / Strength	Strength	Rationale / Clinical Context
	BP6Reputable source reports benign		ClinVar 1-star benign — moderate (BP6); ClinVar germline classification: Benign/Likely Benign, 1 star(s).

Variant Effect in Transcripts

Automated classification analysis was done for transcript: NM_000214.3. You can select a different transcript below to see updated classification assignments.

RefSeq Transcripts

Sel.	Gene / Transcript	Tags	HGVSc / HGVSp	Effect	Exon rank	Protein / UniProt
	JAG1 NM_000214.3	MANE Select	c.388-11_388-8delTTGT	splice_regionintron	Intron 2 of 25	Prot: NP_000205.1 UniProt:

JAG1 NM_000214.3

MANE Select

HGVSc / HGVSpc.388-11_388-8delTTGT

Exon rankIntron 2 of 25

splice_regionintron

Prot: NP_000205.1UniProt: P78504-1

Ensembl Transcripts

Sel.	Gene / Transcript	Tags	HGVSc / HGVSp	Effect	Exon rank	Protein / UniProt
	JAG1 ENST00000254958.10	TSL:1MANE Select	c.388-11_388-8delTTGT	splice_regionintron	Intron 2 of 25	Prot: ENSP00000254958.4 UniProt:
	JAG1 ENST00000901230.1		c.388-11_388-8delTTGT	splice_regionintron	Intron 3 of 26	Prot: ENSP00000571289.1 UniProt:
	JAG1 ENST00000913738.1		c.388-11_388-8delTTGT	splice_regionintron	Intron 2 of 25	Prot: ENSP00000583797.1 UniProt:

JAG1 ENST00000254958.10

TSL:1MANE Select

HGVSc / HGVSpc.388-11_388-8delTTGT

Exon rankIntron 2 of 25

splice_regionintron

Prot: ENSP00000254958.4UniProt: P78504-1

JAG1 ENST00000901230.1

HGVSc / HGVSpc.388-11_388-8delTTGT

Exon rankIntron 3 of 26

splice_regionintron

Prot: ENSP00000571289.1UniProt: P78504-1

JAG1 ENST00000913738.1

HGVSc / HGVSpc.388-11_388-8delTTGT

Exon rankIntron 2 of 25

splice_regionintron

Prot: ENSP00000583797.1UniProt: A0ACI8SNI3

Frequencies

Allele frequencies (AF), counts (AC/AN), homozygotes and coverage

Common (AF > 0.05 / Hom > 5)

Rare (AF ≤ 0.0001 / Hom ≤ 1)

Source / population	AF	AC	Hom	AN	Coverage
Global population databases 6 sources Large-scale international reference populations
GnomAD3 genomes	AF: 0.0000263	AC:4	Hom:0	AN:152170	Cov:32
GnomAD2 exomes	AF: 0.0000517	AC:13	Hom:	AN:251480	Cov:
GnomAD4 exome Warning	AF: 0.0000233	AC:34	Hom:0	AN:1460628	Cov:
GnomAD4 genome	AF: 0.0000263	AC:4	Hom:0	AN:152288	Cov:32
TOPMed (Bravo)	AF: 0.00000378	AC:1	Hom:0	AN:264690	Cov:
ALFA (dbGaP/dbSNP Allele Frequency Aggregator)	AF: 0.0000674	AC:1	Hom:0	AN:14846	Cov:

Showing 6 sources

Case/control cohorts

Cohort	Cases			Controls
	AF	AC	AN	AF	AC	AN
BipEx(Bipolar disorder (including schizoaffective))	0.00	0	28420	0.0000347	1	28844
SCHEMA(Schizophrenia)	0.0000194	2	103316	0.00000542	1	184464

Showing 2 cohortsAllele count / allele number. AF is computed from the counts for ASC (not provided by the source).

ClinVar

ClinVar submissions

Significance: Likely benign

Revision: criteria provided, single submitter

Pathogenic	VUS	Benign	Condition
-	-	1	Alagille syndrome due to a JAG1 point mutation (1)

Computational Scores

Algorithm	Calibrated pred.	Score	Prediction
Mutation Taster	N/A	98/2	polymorphism
PhyloP100	Pathogenic	8.6

Showing 2 of 2 scores

Splicing Scores

Algorithm	Calibrated pred.	Score	Prediction
SpliceAI score (max)	Benign	0.010	Details are displayed if max score is > 0.2

Showing 1 of 1 scores

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

MaveDB functional evidence

MaveDB is a public repository of laboratory assays that test the effect of thousands of variants at once — treat this as supporting research data and interpret it with great caution; it is not a clinical classification.

No MaveDB functional evidence found for this variant.

Other links and lift over

dbSNP: rs750004416;

hg19: chr20-10644669;

ACMG debug oncogenicity

ACGS debug oncogenicity

ACMG debug germline

Submit to ClinVar