Colon Cancer: Gene >> HUNK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270112
Start	31998849:31998849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1810C>T
AA Mutation	p.Pro604Ser(p.P604S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270112
Start	31995858:31995858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1396C>A
AA Mutation	p.Gln466Lys(p.Q466K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270112
Start	31924741:31924741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Trp(p.R179W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270112
Start	31998721:31998721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1682C>G
AA Mutation	p.Ser561Cys(p.S561C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000270112
Start	31995916:31995916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769777844
CDS Mutation	c.1454G>A
AA Mutation	p.Arg485Gln(p.R485Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270112
Start	31946113:31946113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688G>A
AA Mutation	p.Ala230Thr(p.A230T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000270112
Start	31924601:31924601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761716649
CDS Mutation	c.395C>T
AA Mutation	p.Thr132Met(p.T132M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270112
Start	31924749:31924749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270112
Start	31998962:31998962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147755076
CDS Mutation	c.1923G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270112
Start	31999025:31999025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1986G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270112
Start	31958870:31958870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760097878
CDS Mutation	c.774C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270112
Start	31958876:31958876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775557579
CDS Mutation	c.780G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270112
Start	31924501:31924501(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.299delA
AA Mutation	p.Lys100ArgfsTer18(p.K100Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000270112
Start	31924534:31924534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328C>T
AA Mutation	p.Arg110Ter(p.R110*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000270112
Start	31999176:31999176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778884120
CDS Mutation	c.2137C>T
AA Mutation	p.Gln713Ter(p.Q713*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000270112
Start	31999063:31999064(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2025_2030dupCCATCA
AA Mutation	p.His676_Gln677insHisHis(p.H676_Q677insHH)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HUNK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270112
Start	31958887:31958887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576162040
CDS Mutation	c.791C>T
AA Mutation	p.Thr264Met(p.T264M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270112
Start	31968322:31968322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755514543
CDS Mutation	c.947C>T
AA Mutation	p.Ala316Val(p.A316V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270112
Start	31974654:31974654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764724200
CDS Mutation	c.1110C>T
Mutation Classification	Silent
Feature Type	Transcript