Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KRAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245350:25245350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913529
CDS Mutation	c.35G>C
AA Mutation	p.Gly12Ala(p.G12A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245350:25245350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913529
CDS Mutation	c.35G>A
AA Mutation	p.Gly12Asp(p.G12D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25227343:25227343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913238
CDS Mutation	c.181C>A
AA Mutation	p.Gln61Lys(p.Q61K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25227320:25227320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204G>T
AA Mutation	p.Arg68Ser(p.R68S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245351:25245351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913530
CDS Mutation	c.34G>T
AA Mutation	p.Gly12Cys(p.G12C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245350:25245350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913529
CDS Mutation	c.35G>T
AA Mutation	p.Gly12Val(p.G12V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25225713:25225713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351A>T
AA Mutation	p.Lys117Asn(p.K117N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25225628:25225628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913527
CDS Mutation	c.436G>A
AA Mutation	p.Ala146Thr(p.A146T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245347:25245347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112445441
CDS Mutation	c.38G>A
AA Mutation	p.Gly13Asp(p.G13D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25227342:25227342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913240
CDS Mutation	c.182A>G
AA Mutation	p.Gln61Arg(p.Q61R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245351:25245351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913530
CDS Mutation	c.34G>C
AA Mutation	p.Gly12Arg(p.G12R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245348:25245348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913535
CDS Mutation	c.37G>T
AA Mutation	p.Gly13Cys(p.G13C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25225713:25225713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770248150
CDS Mutation	c.351A>C
AA Mutation	p.Lys117Asn(p.K117N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245321:25245321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913236
CDS Mutation	c.64C>A
AA Mutation	p.Gln22Lys(p.Q22K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25225627:25225627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437C>T
AA Mutation	p.Ala146Val(p.A146V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245351:25245351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913530
CDS Mutation	c.34G>A
AA Mutation	p.Gly12Ser(p.G12S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25227341:25227341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17851045
CDS Mutation	c.183A>C
AA Mutation	p.Gln61His(p.Q61H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25215547:25215547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464C>A
AA Mutation	p.Ala155Asp(p.A155D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245328:25245328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.57G>C
AA Mutation	p.Leu19Phe(p.L19F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245284:25245284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104894366
CDS Mutation	c.101C>T
AA Mutation	p.Pro34Leu(p.P34L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25215551:25215551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460G>A
AA Mutation	p.Asp154Asn(p.D154N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256078
Start	25227344:25227344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397517037
CDS Mutation	c.180T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256078
Start	25227344:25227344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000256078
Start	25215550:25215551(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.460_461insTTACATTATA
AA Mutation	p.Asp154ValfsTer4(p.D154Vfs*4)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KRAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245347:25245347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112445441
CDS Mutation	c.38G>A
AA Mutation	p.Gly13Asp(p.G13D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25227349:25227349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913528
CDS Mutation	c.175G>A
AA Mutation	p.Ala59Thr(p.A59T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25227341:25227341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17851045
CDS Mutation	c.183A>T
AA Mutation	p.Gln61His(p.Q61H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25227343:25227343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913238
CDS Mutation	c.181C>G
AA Mutation	p.Gln61Glu(p.Q61E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245350:25245350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913529
CDS Mutation	c.35G>A
AA Mutation	p.Gly12Asp(p.G12D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245350:25245350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913529
CDS Mutation	c.35G>T
AA Mutation	p.Gly12Val(p.G12V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245351:25245351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913530
CDS Mutation	c.34G>T
AA Mutation	p.Gly12Cys(p.G12C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245350:25245350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913529
CDS Mutation	c.35G>C
AA Mutation	p.Gly12Ala(p.G12A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25245351:25245351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913530
CDS Mutation	c.34G>A
AA Mutation	p.Gly12Ser(p.G12S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25227341:25227341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17851045
CDS Mutation	c.183A>C
AA Mutation	p.Gln61His(p.Q61H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25227342:25227342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913240
CDS Mutation	c.182A>T
AA Mutation	p.Gln61Leu(p.Q61L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25225628:25225628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913527
CDS Mutation	c.436G>A
AA Mutation	p.Ala146Thr(p.A146T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000256078
Start	25225713:25225713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351A>T
AA Mutation	p.Lys117Asn(p.K117N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000256078
Start	25245349:25245350(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.30_35dupAGCTGG
AA Mutation	p.Ala11_Gly12dup(p.A11_G12dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript