Colon Cancer: Gene >> INHBA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41700221:41700221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.154C>T
AA Mutation	p.Pro52Ser(p.P52S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41700052:41700052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323G>A
AA Mutation	p.Gly108Glu(p.G108E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41689778:41689778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1153G>T
AA Mutation	p.Ala385Ser(p.A385S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41689883:41689883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048T>C
AA Mutation	p.Cys350Arg(p.C350R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690240:41690240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748226962
CDS Mutation	c.691C>A
AA Mutation	p.Leu231Met(p.L231M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690288:41690288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643A>G
AA Mutation	p.Lys215Glu(p.K215E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41700341:41700341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34G>A
AA Mutation	p.Ala12Thr(p.A12T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41689747:41689747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771243659
CDS Mutation	c.1184A>G
AA Mutation	p.Lys395Arg(p.K395R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41689802:41689802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129C>T
AA Mutation	p.Arg377Cys(p.R377C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690009:41690009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922C>T
AA Mutation	p.Arg308Cys(p.R308C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41700028:41700028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.347T>G
AA Mutation	p.Leu116Arg(p.L116R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690125:41690125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779220866
CDS Mutation	c.806G>A
AA Mutation	p.Gly269Glu(p.G269E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690210:41690210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150182559
CDS Mutation	c.721C>T
AA Mutation	p.Arg241Trp(p.R241W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242208
Start	41700000:41700000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242208
Start	41690178:41690178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776081862
CDS Mutation	c.753C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000242208
Start	41690463:41690463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.468G>A
AA Mutation	p.Trp156Ter(p.W156*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> INHBA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690386:41690386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545C>T
AA Mutation	p.Pro182Leu(p.P182L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690167:41690167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764T>G
AA Mutation	p.Val255Gly(p.V255G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690281:41690281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650C>T
AA Mutation	p.Thr217Ile(p.T217I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690356:41690356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.575C>T
AA Mutation	p.Ala192Val(p.A192V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242208
Start	41690385:41690385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141733287
CDS Mutation	c.546G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242208
Start	41690067:41690067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864G>A
Mutation Classification	Silent
Feature Type	Transcript