chr14:104776711:G>T Detail (hg38) (AKT1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr14:105,243,048-105,243,048 View the variant detail on this assembly version. |
hg38 | chr14:104,776,711-104,776,711 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001014432.1:c.235C>A | NP_001014432.1:p.Gln79Lys |
NM_001014431.1:c.235C>A | NP_001014431.1:p.Gln79Lys | |
NM_005163.2:c.235C>A | NP_005154.2:p.Gln79Lys |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
Clinical Significance |
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Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2014-12-26 | no assertion criteria provided | melanoma |
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Detail |
CIViC
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
The AKT1 Q79K mutation has been shown to confer resistance to BRAF inhibitors (vemurafenib) in melan... | CIViC Evidence | Detail |
In an in vitro study, a M229 cell line endogenously expressing BRAF V600E mutation (a known vemurafe... | CIViC Evidence | Detail |
In a retrospective study of 44 relapsed melanoma patients with BRAF V600E/K (known BRAF inhibitor se... | CIViC Evidence | Detail |
NM_001382430.1(AKT1):c.235C>A (p.Gln79Lys) AND Melanoma | 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
- rs1057519804 dbSNP
- Genome
- hg38
- Position
- chr14:104,776,711-104,776,711
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
- Variant (CIViC) (CIViC Variant)
- Q79K
- Transcript 1 (CIViC Variant)
- ENST00000407796.2
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/169
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