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 Likely pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 164730 OMIM
HGNC 391 HGNC
Ensembl ENSG00000142208 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC COSM159008 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 melanoma somatic Detail
CIViC
Disease Drug EL ET ED CS VO TR Pubmed Links
melanoma Vemurafenib D Predictive Supports Resistance Somatic 4 24265152 Detail
melanoma Vemurafenib D Predictive Supports Resistance Somatic 24265155 Detail
melanoma Dabrafenib C Predictive Supports Resistance Somatic 4 24265155 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
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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