Colon Cancer: Gene >> RASA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87385366:87385366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2824A>C
AA Mutation	p.Asn942His(p.N942H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87333280:87333280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842G>T
AA Mutation	p.Arg281Ile(p.R281I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87376960:87376960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2264T>C
AA Mutation	p.Ile755Thr(p.I755T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87363494:87363494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1600C>A
AA Mutation	p.Leu534Ile(p.L534I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87331389:87331389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.581G>A
AA Mutation	p.Arg194His(p.R194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87353183:87353183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755634472
CDS Mutation	c.1280G>A
AA Mutation	p.Arg427Gln(p.R427Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87376983:87376983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764802465
CDS Mutation	c.2287G>A
AA Mutation	p.Glu763Lys(p.E763K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87385346:87385346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2804A>C
AA Mutation	p.Lys935Thr(p.K935T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87331388:87331388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761101703
CDS Mutation	c.580C>T
AA Mutation	p.Arg194Cys(p.R194C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87376942:87376942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2246G>A
AA Mutation	p.Arg749Gln(p.R749Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87349282:87349282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171C>T
AA Mutation	p.Arg391Trp(p.R391W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87389478:87389478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3011C>T
AA Mutation	p.Ala1004Val(p.A1004V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274376
Start	87380575:87380575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2670C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274376
Start	87349224:87349224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1113C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274376
Start	87362610:87362610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1392T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274376
Start	87379754:87379754(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2513delA
AA Mutation	p.Asn838MetfsTer4(p.N838Mfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000274376
Start	87363446:87363446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1552G>T
AA Mutation	p.Gly518Ter(p.G518*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000274376
Start	87333291:87333291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137853218
CDS Mutation	c.853C>T
AA Mutation	p.Arg285Ter(p.R285*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000274376
Start	87374892:87374892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1987A>T
AA Mutation	p.Lys663Ter(p.K663*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274376
Start	87383720:87383721(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2703dupT
AA Mutation	p.Leu902SerfsTer34(p.L902Sfs*34)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274376
Start	87374311:87374312(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1926_1927insAT
AA Mutation	p.Val643MetfsTer15(p.V643Mfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274376
Start	87374313:87374314(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1927_1928insGGCT
AA Mutation	p.Val643GlyfsTer4(p.V643Gfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000274376
Start	87346671:87346671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1050-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000274376
Start	87268742:87268765(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.296_319delCTGCTGGCGTGGCCGGTGCTGCTG
AA Mutation	p.Ala99_Ala106del(p.A99_A106del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000274376
Start	87362638:87362639(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1425_1426insAAAATTATTTCATACATT
AA Mutation	p.Ile475_Val476insLysIleIleSerTyrIle(p.I475_V476insKIISYI)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000274376
Start	87374891:87374892(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1986_1987insGTGTGC
AA Mutation	p.Thr662_Lys663insValCys(p.T662_K663insVC)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RASA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87374211:87374211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1825A>C
AA Mutation	p.Lys609Gln(p.K609Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87333292:87333292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374823017
CDS Mutation	c.854G>A
AA Mutation	p.Arg285Gln(p.R285Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87385325:87385325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2783G>T
AA Mutation	p.Arg928Ile(p.R928I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274376
Start	87383766:87383766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2744T>G
AA Mutation	p.Phe915Cys(p.F915C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274376
Start	87376997:87376997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751475441
CDS Mutation	c.2301G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000274376
Start	87353188:87353188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285G>T
AA Mutation	p.Glu429Ter(p.E429*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript