Colon Cancer: Gene >> SOX7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304501
Start	10726612:10726612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.293C>T
AA Mutation	p.Ala98Val(p.A98V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304501
Start	10725944:10725944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746671600
CDS Mutation	c.961G>A
AA Mutation	p.Val321Met(p.V321M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304501
Start	10726112:10726112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793T>C
AA Mutation	p.Ser265Pro(p.S265P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304501
Start	10726510:10726510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767524561
CDS Mutation	c.395G>A
AA Mutation	p.Gly132Asp(p.G132D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304501
Start	10726181:10726181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724T>C
AA Mutation	p.Tyr242His(p.Y242H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304501
Start	10726448:10726448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142748053
CDS Mutation	c.457C>T
AA Mutation	p.Arg153Trp(p.R153W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304501
Start	10725831:10725831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304501
Start	10725927:10725927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529374931
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304501
Start	10730257:10730257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304501
Start	10725909:10725909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.996C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304501
Start	10726136:10726136(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.769delC
AA Mutation	p.Leu257TrpfsTer14(p.L257Wfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SOX7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304501
Start	10726516:10726516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389A>G
AA Mutation	p.Asp130Gly(p.D130G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304501
Start	10726523:10726523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747827752
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Cys(p.R128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304501
Start	10725920:10725920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749229532
CDS Mutation	c.985C>T
AA Mutation	p.Arg329Cys(p.R329C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304501
Start	10725909:10725909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.996C>T
Mutation Classification	Silent
Feature Type	Transcript