chr9:130872946:C>T Detail (hg38) (ABL1)

Information

Genome

Assembly Position
hg19 chr9:133,748,333-133,748,333 View the variant detail on this assembly version.
hg38 chr9:130,872,946-130,872,946

HGVS

Type Transcript Protein
RefSeq NM_005157.5:c.994C>T NP_005148.2:p.Arg332Trp
NM_007313.2:c.1051C>T NP_009297.2:p.Arg351Trp
Ensemble ENST00000318560.6:c.994C>T ENST00000318560.6:p.Arg332Trp
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:[No Data.]
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:<0.001

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
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 COSM1176546 COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease Drug EL ET ED CS VO TR Pubmed Links
lung non-small cell carcinoma Dasatinib D Predictive Supports Sensitivity/Response Somatic 4 26758680 Detail
lung non-small cell carcinoma Imatinib D Predictive Supports Sensitivity/Response Somatic 5 26758680 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
In this in vitro study, the H1915 non-small cell lung cancer cell line (homozygous for a R351W mutat... CIViC Evidence Detail
In this in vitro study, the H1915 non-small cell lung cancer cell line (homozygous for a R351W mutat... CIViC Evidence 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
-
Genome
hg38
Position
chr9:130,872,946-130,872,946
Variant Type
snv
Reference Allele
C
Alternative Allele
T
East Asian Chromosome Counts (ExAC)
8654
East Asian Allele Counts (ExAC)
0
East Asian Heterozygous Counts (ExAC)
0
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
0.0
Chromosome Counts in All Race (ExAC)
121366
Allele Counts in All Race (ExAC)
1
Heterozygous Counts in All Race (ExAC)
1
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
8.239539904091756E-6
Variant (CIViC) (CIViC Variant)
R351W
Transcript 1 (CIViC Variant)
ENST00000372348.2
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/1656
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