NM_002055.5:c.883G>A

Variant names:

Variant summary

Our verdict is Benign. The variant received -20 ACMG points: 0P and 20B. BP4_StrongBP6_Very_StrongBA1

The NM_002055.5(GFAP):c.883G>A(p.Asp295Asn) variant causes a missense change. The variant allele was found at a frequency of 0.0421 in 1,613,504 control chromosomes in the GnomAD database, including 1,847 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

Frequency

Genomes: 𝑓 0.036 ( 152 hom., cov: 33)

Exomes 𝑓: 0.043 ( 1695 hom. )

Consequence

GFAP
NM_002055.5 missense

Scores

Clinical Significance

Benign criteria provided, multiple submitters, no conflicts B:5O:1

Conservation

PhyloP100: 6.17

Publications

24 publications found

Variant links:

Genes affected

GFAP (HGNC:4235): (glial fibrillary acidic protein) This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]

GFAP Gene-Disease associations (from GenCC):

Alexander disease
Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: Genomics England PanelApp, Labcorp Genetics (formerly Invitae), ClinGen, G2P
Alexander disease type II
Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet

GFAP links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -20 ACMG points.

BP4

Computational evidence support a benign effect (MetaRNN=0.003569454).

BP6

Variant 17-44911695-C-T is Benign according to our data. Variant chr17-44911695-C-T is described in ClinVar as Benign. ClinVar VariationId is 66509.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BA1

GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.133 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_002055.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
GFAP	NM_002055.5	MANE Select	c.883G>A	p.Asp295Asn	missense	Exon 5 of 9	NP_002046.1	P14136-1
GFAP	NM_001363846.2		c.883G>A	p.Asp295Asn	missense	Exon 5 of 10	NP_001350775.1	A0A1X7SBR3
GFAP	NM_001242376.3		c.883G>A	p.Asp295Asn	missense	Exon 5 of 7	NP_001229305.1	P14136-2

Ensembl Transcripts

Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
GFAP	ENST00000588735.3	TSL:1 MANE Select	c.883G>A	p.Asp295Asn	missense	Exon 5 of 9	ENSP00000466598.2	P14136-1
GFAP	ENST00000591327.2	TSL:1	n.2037G>A		non_coding_transcript_exon	Exon 3 of 5
GFAP	ENST00000639277.1	TSL:5	c.883G>A	p.Asp295Asn	missense	Exon 5 of 10	ENSP00000492432.1	A0A1W2PR46

Frequencies

GnomAD3 genomes

AF:

0.0356

AC:

5419

AN:

152234

Hom.:

147

Cov.:

show subpopulations

Gnomad AFR

AF:

0.0223

Gnomad AMI

AF:

0.00219

Gnomad AMR

AF:

0.0279

Gnomad ASJ

AF:

0.0478

Gnomad EAS

AF:

0.141

Gnomad SAS

AF:

0.0602

Gnomad FIN

AF:

0.0140

Gnomad MID

AF:

0.00316

Gnomad NFE

AF:

0.0393

Gnomad OTH

AF:

0.0239

GnomAD2 exomes

AF:

0.0454

AC:

11291

AN:

248574

AF XY:

0.0458

show subpopulations

Gnomad AFR exome

AF:

0.0211

Gnomad AMR exome

AF:

0.0417

Gnomad ASJ exome

AF:

0.0461

Gnomad EAS exome

AF:

0.143

Gnomad FIN exome

AF:

0.0129

Gnomad NFE exome

AF:

0.0373

Gnomad OTH exome

AF:

0.0353

GnomAD4 exome

AF:

0.0428

AC:

62509

AN:

1461152

Hom.:

1695

Cov.:

AF XY:

0.0428

AC XY:

31148

AN XY:

726966

show subpopulations

African (AFR)

AF:

0.0198

AC:

663

AN:

33476

American (AMR)

AF:

0.0428

AC:

1915

AN:

44710

Ashkenazi Jewish (ASJ)

AF:

0.0454

AC:

1184

AN:

26106

East Asian (EAS)

AF:

0.147

AC:

5848

AN:

39686

South Asian (SAS)

AF:

0.0566

AC:

4885

AN:

86236

European-Finnish (FIN)

AF:

0.0145

AC:

768

AN:

52992

Middle Eastern (MID)

AF:

0.0209

AC:

120

AN:

5740

European-Non Finnish (NFE)

AF:

0.0401

AC:

44585

AN:

1111830

Other (OTH)

AF:

0.0421

AC:

2541

AN:

60376

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.433

Heterozygous variant carriers

3525

7051

10576

14102

17627

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Exome Hom

Variant carriers

1802

3604

5406

7208

9010

<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:

0.0356

AC:

5428

AN:

152352

Hom.:

152

Cov.:

AF XY:

0.0349

AC XY:

2603

AN XY:

74498

show subpopulations

African (AFR)

AF:

0.0223

AC:

926

AN:

41590

American (AMR)

AF:

0.0286

AC:

437

AN:

15306

Ashkenazi Jewish (ASJ)

AF:

0.0478

AC:

166

AN:

3470

East Asian (EAS)

AF:

0.141

AC:

731

AN:

5178

South Asian (SAS)

AF:

0.0598

AC:

289

AN:

4830

European-Finnish (FIN)

AF:

0.0140

AC:

149

AN:

10626

Middle Eastern (MID)

AF:

0.00340

AC:

AN:

294

European-Non Finnish (NFE)

AF:

0.0393

AC:

2677

AN:

68032

Other (OTH)

AF:

0.0237

AC:

AN:

2114

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.498

Heterozygous variant carriers

276

552

829

1105

1381

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome Het

Genome Hom

Variant carriers

148

222

296

370

<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:

0.0403

Hom.:

609

Bravo

AF:

0.0369

TwinsUK

AF:

0.0429

AC:

159

ALSPAC

AF:

0.0444

AC:

171

ESP6500AA

AF:

0.0223

AC:

ESP6500EA

AF:

0.0377

AC:

324

ExAC

AF:

0.0447

AC:

5422

Asia WGS

AF:

0.0950

AC:

331

AN:

3478

EpiCase

AF:

0.0358

EpiControl

AF:

0.0311

ClinVar

ClinVar submissions

Significance:Benign

Revision:criteria provided, multiple submitters, no conflicts

View on ClinVar

Pathogenic

VUS

Benign

Condition

not provided (6)

Computational scores

Source: dbNSFP v4.9

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Uncertain

0.34

BayesDel_addAF

Benign

-0.40

BayesDel_noAF

Benign

-0.24

CADD

Pathogenic

(source)

DANN

Uncertain

1.0

DEOGEN2

Pathogenic

0.81

Eigen

Uncertain

0.44

Eigen_PC

Uncertain

0.34

FATHMM_MKL

Uncertain

0.93

LIST_S2

Pathogenic

0.98

MetaRNN

Benign

0.0036

MetaSVM

Benign

-0.65

MutationAssessor

Uncertain

2.5

PhyloP100

6.2

PrimateAI

Uncertain

0.63

PROVEAN

Uncertain

-2.7

REVEL

Uncertain

0.51

Sift

Pathogenic

0.0

Sift4G

Pathogenic

0.0010

Polyphen

0.99

Vest4

0.36

MPC

1.2

ClinPred

0.015

GERP RS

3.4

PromoterAI

-0.018

Neutral

(source)

Varity_R

0.83

gMVP

0.96

Mutation Taster

=72/28

polymorphism (auto)

(source)

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

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Variant Effect in Transcripts

RefSeq Transcripts

Ensembl Transcripts

Frequencies

Age Distribution

Age Distribution

ClinVar

Computational scores

Splicing

Publications

Other links and lift over