Colon Cancer: Gene >> ISL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51384709:51384709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.197A>G
AA Mutation	p.Tyr66Cys(p.Y66C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51387704:51387704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.433G>A
AA Mutation	p.Asp145Asn(p.D145N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51389796:51389796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629T>A
AA Mutation	p.Met210Lys(p.M210K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51389865:51389865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.698G>A
AA Mutation	p.Arg233Gln(p.R233Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51387639:51387639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368G>A
AA Mutation	p.Arg123Gln(p.R123Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51387501:51387501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230T>A
AA Mutation	p.Ile77Asn(p.I77N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51387626:51387626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Glu119Lys(p.E119K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51387687:51387687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416C>A
AA Mutation	p.Ala139Asp(p.A139D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51389864:51389864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.697C>T
AA Mutation	p.Arg233Trp(p.R233W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51389924:51389924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.757G>C
AA Mutation	p.Asp253His(p.D253H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51387684:51387684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413G>T
AA Mutation	p.Arg138Met(p.R138M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51393510:51393510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.950G>A
AA Mutation	p.Gly317Glu(p.G317E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230658
Start	51391393:51391393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41268419
CDS Mutation	c.885C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230658
Start	51389674:51389674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000230658
Start	51389882:51389882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715C>T
AA Mutation	p.Arg239Ter(p.R239*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ISL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230658
Start	51391283:51391283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.775G>C
AA Mutation	p.Gly259Arg(p.G259R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230658
Start	51387544:51387544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript