chr9:133748288:T>G Detail (hg19) (ABL1)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr9:133,748,288-133,748,288
hg38	chr9:130,872,901-130,872,901 View the variant detail on this assembly version.

HGVS

ABL1

Type	Transcript	Protein
RefSeq	NM_005157.5:c.949T>G	NP_005148.2:p.Phe317Val
	NM_007313.2:c.1006T>G	NP_009297.2:p.Phe336Val
Ensemble	ENST00000318560.6:c.949T>G	ENST00000318560.6:p.Phe317Val
	ENST00000372348.9:c.1006T>G	ENST00000372348.9:p.Phe336Val

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Likely pathogenic
Review star
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Links

ABL1

Type	Database	ID	Link
Gene	MIM	189980	OMIM
	HGNC	76	HGNC
	Ensembl	ENSG00000097007	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC	COSM211607	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Likely pathogenic	2014-12-26	no assertion criteria provided	chronic myelogenous leukemia, BCR-ABL1 positive	somatic	Detail

CIViC

Disease	Drug	EL	ET	ED	CS	VO	TR	Pubmed	Links
chronic myeloid leukemia	Axitinib	D	Predictive	Supports	Resistance	Somatic	2	25686603	Detail
chronic myeloid leukemia	Dasatinib	D	Predictive	Supports	Resistance	Somatic	3	15705718	Detail
chronic myeloid leukemia	Dasatinib	D	Predictive	Supports	Resistance	Somatic	2	16772610	Detail

DisGeNET

[No Data.]

Annotation

Annotations

Descrption	Source	Links
In a proliferation assay measuring tritiated thymidine incorporation in the presence of axitinib, Ba...	CIViC Evidence	Detail
In an in vitro study, stochastic mutations in the ABL1 region of a stably expressed p210 BCR-ABL fus...	CIViC Evidence	Detail
In an in vitro study, stochastic mutations were introduced into the ABL1 region of a stably expresse...	CIViC Evidence	Detail
NM_005157.6(ABL1):c.949T>G (p.Phe317Val) AND Chronic myelogenous leukemia, BCR-ABL1 positive	ClinVar	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs1057519773 dbSNP
Genome: hg19
Position: chr9:133,748,288-133,748,288
Variant Type: snv
Reference Allele: T
Alternative Allele: G
Variant (CIViC) (CIViC Variant): BCR-ABL F317V
Transcript 1 (CIViC Variant): ENST00000318560.5
Variant URL (CIViC Variant): https://civic.genome.wustl.edu/links/variants/1525

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