1-4712438-G-A

Variant names:

• chr1-4712438-G-A
• rs764876909
• NM_018836.4:c.568G>A
• AJAP1 p.Glu190Lys

GermlineCancer (beta)

Variant summary

Our verdict is Likely benign.

-1 Likely Benign

-7

-6

-1

0

+5

+6

+9

+10

BenignB

Likely BenignLB

UncertainVUS

Likely PathogenicLP

PathogenicP

The variant received -1 classification points (ACMG Germline Pathogenicity v2019). PM2_SupportingBP4_Moderate

The NM_018836.4(AJAP1):c.568G>A (p.Glu190Lys) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a cumulative frequency of 0.00000206 (AC=3) in the gnomAD database across 1,454,590 control chromosomes (no homozygotes observed). The grpmax filtering allele frequency (95% CI) is 0.0000181. In-silico predictor (REVEL) classifies this variant as likely benign. Splicing prediction tools (SpliceAI) predict no significant impact on normal splicing. Variant has been reported in ClinVar as Uncertain Significance (★).

• Frequency:
  • Genomes: not found (cov: 33)
  • Exomes 𝑓: 0.0000021 (0 hom.)
• Consequence: AJAP1 NM_018836.4 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 2.42
• Publications: 1 publications found

Genes affected

AJAP1 (HGNC:30801): (adherens junctions associated protein 1) Enables beta-catenin binding activity. Involved in negative regulation of cell-matrix adhesion; negative regulation of wound healing; and regulation of polarized epithelial cell differentiation. Located in several cellular components, including adherens junction; basolateral plasma membrane; and cell-cell contact zone. [provided by Alliance of Genome Resources, Jul 2025]

AJAP1 Gene-Disease associations (from GenCC):

• neurodevelopmental disorder

  Inheritance: AD Classification: STRONG Submitted by: PanelApp Australia

Classification according to ACMG Germline Pathogenicity v2019

Classification was made for transcript:

Our verdict: Likely_benign. The variant received -1 points.

Apply	Criterion Code & Title / Strength	Strength	Rationale / Clinical Context
	PM2Absent/extremely low in population databases		Rare in gnomAD for AD/XL gene (popmax AF below threshold) — PM2 Supporting; GnomAD popmax AF = 0.0000181 — borderline rare for AD/XL gene (threshold 0.0001) — PM2 supporting.
	BP4Computational evidence suggests no impact		Computational evidence supports benign — no pathogenic computational or splicing signal (BP4); Splicing verdict: benign (Strong).; Germline computational verdict: benign (Moderate).

Variant Effect in Transcripts

Automated classification analysis was done for transcript: NM_018836.4. 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
	AJAP1 NM_018836.4	MANE Select	c.568G>A p.Glu190Lys	missense	Exon 2 of 6	Prot: NP_061324.1 UniProt:
	AJAP1 NM_001042478.2		c.568G>A p.Glu190Lys	missense	Exon 2 of 6	Prot: NP_001035943.1 UniProt:

AJAP1 NM_018836.4

MANE Select

HGVSc / HGVSpc.568G>Ap.Glu190Lys

Exon rankExon 2 of 6

missense

Prot: NP_061324.1UniProt: Q9UKB5

AJAP1 NM_001042478.2

HGVSc / HGVSpc.568G>Ap.Glu190Lys

Exon rankExon 2 of 6

missense

Prot: NP_001035943.1UniProt: Q9UKB5

Ensembl Transcripts

Sel.	Gene / Transcript	Tags	HGVSc / HGVSp	Effect	Exon rank	Protein / UniProt
	AJAP1 ENST00000378191.5	TSL:1MANE Select	c.568G>A p.Glu190Lys	missense	Exon 2 of 6	Prot: ENSP00000367433.3 UniProt:
	AJAP1 ENST00000378190.7	TSL:5	c.568G>A p.Glu190Lys	missense	Exon 2 of 6	Prot: ENSP00000367432.3 UniProt:
	AJAP1 ENST00000880749.1		c.568G>A p.Glu190Lys	missense	Exon 2 of 5	Prot: ENSP00000550808.1 UniProt:

AJAP1 ENST00000378191.5

TSL:1MANE Select

HGVSc / HGVSpc.568G>Ap.Glu190Lys

Exon rankExon 2 of 6

missense

Prot: ENSP00000367433.3UniProt: Q9UKB5

AJAP1 ENST00000378190.7

TSL:5

HGVSc / HGVSpc.568G>Ap.Glu190Lys

Exon rankExon 2 of 6

missense

Prot: ENSP00000367432.3UniProt: Q9UKB5

AJAP1 ENST00000880749.1

HGVSc / HGVSpc.568G>Ap.Glu190Lys

Exon rankExon 2 of 5

missense

Prot: ENSP00000550808.1UniProt: Q9UKB5

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:	AC:	Hom:	AN:	Cov:33
GnomAD2 exomes	AF: 0.0000127	AC:3	Hom:	AN:235578	Cov:
GnomAD4 exome	AF: 0.00000206	AC:3	Hom:0	AN:1454590	Cov:37
GnomAD4 genome	AF:	AC:	Hom:	AN:	Cov:33
TOPMed (Bravo)	AF: 0.00000378	AC:	Hom:	AN:	Cov:
ALFA (dbGaP/dbSNP Allele Frequency Aggregator)	AF: 0.00	AC:0	Hom:0	AN:16840	Cov:

Showing 6 sources

Case/control cohorts

Cohort	Cases			Controls
	AF	AC	AN	AF	AC	AN
Epi25(Epilepsy)	0.00	0	41836	0.0000150	1	66730
SCHEMA(Schizophrenia)	0.0000199	2	100336	0.00000555	1	180132

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

ClinVar

ClinVar submissions

Significance: Uncertain significance

Revision: criteria provided, single submitter

Pathogenic	VUS	Benign	Condition
-	1	-	not specified (1)

Computational Scores

Algorithm	Calibrated pred.	Score	Prediction
AlphaGenome AVI	Pathogenic	23
AlphaMissense	Benign	0.22
BayesDel_addAF	Benign	-0.22	T
BayesDel_noAF	Benign	-0.35
CADD	Pathogenic	27
DANN	Uncertain	1.0
DEOGEN2	Benign	0.12	T
Eigen	Benign	-0.039
Eigen_PC	Benign	0.091
FATHMM_MKL	Uncertain	0.80	D
FuncVEP CTI	Benign	0.065
GPN-Star LLR	N/A	-8.6
GPN-Star score	N/A	8.6
LIST_S2	Benign	0.85	T
M_CAP	Benign	0.011	T
MetaRNN	Benign	0.15	T
MetaSVM	Benign	-0.85	T
Mutation Taster	N/A	90/10	polymorphism
MutationAssessor	Benign	1.6	L
PhyloP100	Benign	2.4
popEVE	Benign	-3.3
PrimateAI	Uncertain	0.53	T
PROVEAN	Uncertain	-3.0	D
REVEL	Benign	0.11
Sift	Uncertain	0.018	D
Sift4G	Benign	0.073	T
Varity_R	N/A	0.35
VESM-3B	Benign	-7.1

Showing 28 of 28 scores

Splicing Scores

Algorithm	Calibrated pred.	Score	Prediction
Pangolin (max)	Benign	0.0
SpliceAI score (max)	Benign	0.0	Details are displayed if max score is > 0.2

Showing 2 of 2 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: rs764876909;

hg19: chr1-4772498;

ACMG debug oncogenicity

ACGS debug oncogenicity

ACMG debug germline

Submit to ClinVar