chr7:140481403:C>T Detail (hg19) (BRAF)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr7:140,481,403-140,481,403 |
hg38 | chr7:140,781,603-140,781,603 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_004333.4:c.1525G>A | NP_004324.2:p.Gly509Arg |
Ensemble | ENST00000288602.11:c.1525G>A | ENST00000288602.11:p.Gly509Arg |
ENST00000496384.7:c.1405G>A | ENST00000496384.7:p.Gly469Arg |
Summary
MGeND
Clinical significance |
![]() |
Variant entry | 1 |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
Clinical Significance |
![]() ![]() |
Review star | ![]() |
Show details |
Disease area statistics
MGeND
Clinical significance | Last evaluated | Condition | Origin | Submission ID | Submitter | Institute | Citation | Comment | Image |
---|---|---|---|---|---|---|---|---|---|
![]() |
descending colon |
![]() |
MGS000041
(TMGS000094) |
Hitoshi Nakagama | National Cancer Center Japan |
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
![]() |
2013-10-10 | criteria provided, single submitter | Non-small cell lung carcinoma |
![]() |
Detail |
![]() |
2015-07-14 | no assertion criteria provided | melanoma |
![]() |
Detail |
![]() |
2020-07-01 | criteria provided, single submitter | Noonan syndrome and Noonan-related syndrome |
![]() |
Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.242 | Lymphoma, Non-Hodgkin | NA | CLINVAR | Detail | |
0.131 | Non-small cell lung carcinoma | We present a case report of a patient with NSCLC and the BRAF G469R mutation who... | BeFree | 26237499 | Detail |
0.131 | Non-small cell lung carcinoma | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_004333.6(BRAF):c.1405G>A (p.Gly469Arg) AND Non-small cell lung carcinoma | ClinVar | Detail |
NM_004333.6(BRAF):c.1405G>A (p.Gly469Arg) AND Melanoma | ClinVar | Detail |
NM_004333.6(BRAF):c.1405G>A (p.Gly469Arg) AND Noonan syndrome and Noonan-related syndrome | ClinVar | Detail |
NA | DisGeNET | Detail |
We present a case report of a patient with NSCLC and the BRAF G469R mutation who showed a dramatic r... | DisGeNET | Detail |
NA | DisGeNET | 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
- rs121913357 dbSNP
- Genome
- hg19
- Position
- chr7:140,481,403-140,481,403
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
Genome browser