Colon Cancer: Gene >> SF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377390
Start	64767585:64767585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1328G>A
AA Mutation	p.Gly443Asp(p.G443D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377390
Start	64776558:64776558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100C>T
AA Mutation	p.Pro34Ser(p.P34S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377390
Start	64766020:64766020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1718T>G
AA Mutation	p.Val573Gly(p.V573G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377390
Start	64769269:64769269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111552365
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Trp(p.R245W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377390
Start	64768153:64768153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021G>A
AA Mutation	p.Ala341Thr(p.A341T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377390
Start	64769238:64769238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.764G>A
AA Mutation	p.Arg255Gln(p.R255Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377390
Start	64776521:64776521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773401736
CDS Mutation	c.137G>A
AA Mutation	p.Arg46Gln(p.R46Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377390
Start	64766112:64766112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1626G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377390
Start	64765941:64765941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1797G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377390
Start	64766946:64766946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201418411
CDS Mutation	c.1536G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377390
Start	64767039:64767039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564895500
CDS Mutation	c.1443G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377390
Start	64768148:64768148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753308456
CDS Mutation	c.1026C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377390
Start	64773445:64773445(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.221delC
AA Mutation	p.Pro74LeufsTer63(p.P74Lfs*63)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377390
Start	64766025:64766025(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1713delC
AA Mutation	p.Val573SerfsTer23(p.V573Sfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377390
Start	64769552:64769552(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.537delG
AA Mutation	p.Ser182LeufsTer2(p.S182Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000377390
Start	64768240:64768240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934G>T
AA Mutation	p.Glu312Ter(p.E312*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000377390
Start	64776624:64776625(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.33_34insCTATATAAGCTCTTTCTTG
AA Mutation	p.Phe12LeufsTer10(p.F12Lfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377390
Start	64769568:64769568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521A>C
AA Mutation	p.Lys174Thr(p.K174T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript