Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RHOA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000418115
Start	49368499:49368499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206T>C
AA Mutation	p.Leu69Pro(p.L69P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000418115
Start	49375475:49375475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.115T>C
AA Mutation	p.Phe39Leu(p.F39L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000418115
Start	49368523:49368523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.182C>T
AA Mutation	p.Ala61Val(p.A61V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000418115
Start	49375576:49375576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11552758
CDS Mutation	c.14G>A
AA Mutation	p.Arg5Gln(p.R5Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000418115
Start	49368429:49368430(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.275_276delTA
AA Mutation	p.Leu92Ter(p.L92*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000418115
Start	49368451:49368452(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.253dupT
AA Mutation	p.Ser85PhefsTer6(p.S85Ffs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000418115
Start	49375433:49375433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RHOA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000418115
Start	49360330:49360330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461T>G
AA Mutation	p.Phe154Cys(p.F154C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000418115
Start	49362540:49362540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Trp(p.R122W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000418115
Start	49375544:49375544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.46T>A
AA Mutation	p.Cys16Ser(p.C16S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript