Colon Cancer: Gene >> INTS7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	211946642:211946642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2380T>A
AA Mutation	p.Tyr794Asn(p.Y794N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	211981129:211981129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1194T>G
AA Mutation	p.Ser398Arg(p.S398R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	212016964:212016964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147767700
CDS Mutation	c.431G>A
AA Mutation	p.Arg144His(p.R144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	211975362:211975362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1619A>G
AA Mutation	p.Asp540Gly(p.D540G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	211982690:211982690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1118C>A
AA Mutation	p.Ser373Tyr(p.S373Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	211941967:211941967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2746A>G
AA Mutation	p.Ile916Val(p.I916V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	211978405:211978405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780657722
CDS Mutation	c.1337G>A
AA Mutation	p.Arg446Gln(p.R446Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	211946633:211946633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2389C>A
AA Mutation	p.Gln797Lys(p.Q797K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	211978303:211978303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1439G>A
AA Mutation	p.Arg480Gln(p.R480Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	211968527:211968527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778955780
CDS Mutation	c.1996C>T
AA Mutation	p.Arg666Cys(p.R666C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	211944846:211944846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2539A>T
AA Mutation	p.Ile847Phe(p.I847F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	212016979:212016979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416C>T
AA Mutation	p.Ala139Val(p.A139V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366994
Start	211952595:211952595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2290C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366994
Start	211975235:211975235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1746T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366994
Start	212020133:212020133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366994
Start	211946635:211946635(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2387delT
AA Mutation	p.Phe796SerfsTer34(p.F796Sfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366994
Start	212020168:212020168(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.325delT
AA Mutation	p.Ser109LeufsTer2(p.S109Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000366994
Start	211982768:211982768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040T>A
AA Mutation	p.Leu347Ter(p.L347*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000366994
Start	211976623:211976623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1567G>T
AA Mutation	p.Gly523Ter(p.G523*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> INTS7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	212020176:212020176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317G>T
AA Mutation	p.Arg106Ile(p.R106I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366994
Start	211975193:211975193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1788C>A
AA Mutation	p.Phe596Leu(p.F596L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript