Colon Cancer: Gene >> SNED1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241065469:241065469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376117940
CDS Mutation	c.2884C>T
AA Mutation	p.Arg962Cys(p.R962C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241034595:241034595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758442640
CDS Mutation	c.670C>T
AA Mutation	p.Arg224Cys(p.R224C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241049036:241049036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1519C>T
AA Mutation	p.Pro507Ser(p.P507S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241051789:241051789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751414477
CDS Mutation	c.1781C>T
AA Mutation	p.Thr594Met(p.T594M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241052082:241052082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774223730
CDS Mutation	c.1894G>A
AA Mutation	p.Gly632Ser(p.G632S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241082295:241082295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577568792
CDS Mutation	c.4052G>A
AA Mutation	p.Arg1351His(p.R1351H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241053210:241053210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770274133
CDS Mutation	c.2141C>T
AA Mutation	p.Thr714Met(p.T714M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241052433:241052433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2048G>A
AA Mutation	p.Cys683Tyr(p.C683Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241081730:241081730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3970C>T
AA Mutation	p.Pro1324Ser(p.P1324S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241030405:241030405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371291064
CDS Mutation	c.335G>A
AA Mutation	p.Arg112His(p.R112H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241053314:241053314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2245C>T
AA Mutation	p.Pro749Ser(p.P749S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241087453:241087453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4183A>C
AA Mutation	p.Ser1395Arg(p.S1395R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241064934:241064934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759761274
CDS Mutation	c.2690A>G
AA Mutation	p.Tyr897Cys(p.Y897C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241053171:241053171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750356654
CDS Mutation	c.2102C>T
AA Mutation	p.Pro701Leu(p.P701L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241081735:241081735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752905522
CDS Mutation	c.3975C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241040121:241040121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1092C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241048750:241048750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1488G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241064941:241064941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2697C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241082306:241082306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4063A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241033836:241033836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755055045
CDS Mutation	c.603C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241065498:241065498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767178300
CDS Mutation	c.2913G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241052150:241052150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569737866
CDS Mutation	c.1962C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241071874:241071874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3813A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241030487:241030487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769755879
CDS Mutation	c.417C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000310397
Start	241071576:241071576(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3594delC
AA Mutation	p.Arg1199GlyfsTer58(p.R1199Gfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310397
Start	241052361:241052361(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1980delC
AA Mutation	p.Cys661AlafsTer7(p.C661Afs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310397
Start	241073313:241073313(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3865delC
AA Mutation	p.Arg1289GlyfsTer59(p.R1289Gfs*59)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SNED1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241040141:241040141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750619657
CDS Mutation	c.1112C>T
AA Mutation	p.Ala371Val(p.A371V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310397
Start	241087454:241087454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4184G>A
AA Mutation	p.Ser1395Asn(p.S1395N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241062888:241062888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372698242
CDS Mutation	c.2355C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241049059:241049059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1542C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310397
Start	241071871:241071871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3810G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000310397
Start	241036844:241036852(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.860_868delACTGCGTCA
AA Mutation	p.Asp287_Thr290delinsAla(p.D287_T290delinsA)
Mutation Classification	In_Frame_Del
Feature Type	Transcript