Colon Cancer: Gene >> INPPL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72237194:72237194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2950C>A
AA Mutation	p.Pro984Thr(p.P984T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72237170:72237170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2926C>T
AA Mutation	p.Pro976Ser(p.P976S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72235856:72235856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780472220
CDS Mutation	c.2749C>T
AA Mutation	p.Arg917Cys(p.R917C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72233666:72233666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2134G>A
AA Mutation	p.Asp712Asn(p.D712N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72230430:72230430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778197564
CDS Mutation	c.1159C>T
AA Mutation	p.Arg387Trp(p.R387W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72232705:72232705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753557940
CDS Mutation	c.1792C>T
AA Mutation	p.Arg598Cys(p.R598C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72235419:72235419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367743824
CDS Mutation	c.2627C>T
AA Mutation	p.Thr876Met(p.T876M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72232660:72232660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1747C>T
AA Mutation	p.Leu583Phe(p.L583F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72230439:72230439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771324555
CDS Mutation	c.1168C>T
AA Mutation	p.Arg390Cys(p.R390C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72230206:72230206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774794017
CDS Mutation	c.1025G>A
AA Mutation	p.Arg342Gln(p.R342Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72235379:72235379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2587A>G
AA Mutation	p.Thr863Ala(p.T863A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72237164:72237164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2920G>C
AA Mutation	p.Ala974Pro(p.A974P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72237270:72237270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3026T>C
AA Mutation	p.Val1009Ala(p.V1009A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72231130:72231130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438G>A
AA Mutation	p.Glu480Lys(p.E480K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72237668:72237668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374001069
CDS Mutation	c.3424C>T
AA Mutation	p.Arg1142Cys(p.R1142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72229941:72229941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.861G>T
AA Mutation	p.Gln287His(p.Q287H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000298229
Start	72237711:72237711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773081790
CDS Mutation	c.3467G>A
AA Mutation	p.Arg1156Gln(p.R1156Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298229
Start	72232680:72232680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1767G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298229
Start	72228470:72228470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.369G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298229
Start	72228211:72228211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298229
Start	72228758:72228758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298229
Start	72232919:72232919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1896C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298229
Start	72231129:72231129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201505175
CDS Mutation	c.1437C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298229
Start	72237704:72237704(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs764259451
CDS Mutation	c.3466delC
AA Mutation	p.Arg1156GlyfsTer46(p.R1156Gfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298229
Start	72237165:72237165(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2927delC
AA Mutation	p.Pro976HisfsTer155(p.P976Hfs*155)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000298229
Start	72235734:72235734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781674896
CDS Mutation	c.2719C>T
AA Mutation	p.Arg907Ter(p.R907*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000298229
Start	72228462:72228462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361C>T
AA Mutation	p.Arg121Ter(p.R121*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298229
Start	72237164:72237165(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs749079348
CDS Mutation	c.2927dupC
AA Mutation	p.Pro977ThrfsTer7(p.P977Tfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> INPPL1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298229
Start	72235864:72235864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2757A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298229
Start	72237704:72237704(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs764259451
CDS Mutation	c.3466delC
AA Mutation	p.Arg1156GlyfsTer46(p.R1156Gfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript