Colon Cancer: Gene >> MAD1L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	2219447:2219447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749337220
CDS Mutation	c.481G>A
AA Mutation	p.Ala161Thr(p.A161T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	1816215:1816215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577277453
CDS Mutation	c.2012C>T
AA Mutation	p.Ser671Leu(p.S671L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	1936768:1936768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771673407
CDS Mutation	c.1726C>T
AA Mutation	p.Arg576Cys(p.R576C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	1898264:1898264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757932885
CDS Mutation	c.1934C>T
AA Mutation	p.Thr645Met(p.T645M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	1898337:1898337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1861G>C
AA Mutation	p.Val621Leu(p.V621L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	2219405:2219405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523G>T
AA Mutation	p.Asp175Tyr(p.D175Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	1816159:1816159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2068A>G
AA Mutation	p.Ile690Val(p.I690V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	1936780:1936780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752885094
CDS Mutation	c.1714C>T
AA Mutation	p.Arg572Cys(p.R572C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	2216166:2216166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754840623
CDS Mutation	c.800C>T
AA Mutation	p.Ala267Val(p.A267V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	1898286:1898286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746065050
CDS Mutation	c.1912G>A
AA Mutation	p.Gly638Ser(p.G638S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	2215980:2215980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829G>A
AA Mutation	p.Gly277Arg(p.G277R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	2230027:2230027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776910007
CDS Mutation	c.107C>T
AA Mutation	p.Ser36Leu(p.S36L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	2222723:2222723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200930173
CDS Mutation	c.323C>T
AA Mutation	p.Thr108Met(p.T108M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265854
Start	1957695:1957695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1530C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000265854
Start	2222643:2222643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.403C>T
AA Mutation	p.Gln135Ter(p.Q135*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000265854
Start	2219374:2219374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554C>A
AA Mutation	p.Ser185Ter(p.S185*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000265854
Start	2213247:2213247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.951G>A
AA Mutation	p.Trp317Ter(p.W317*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAD1L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	1936832:1936832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1662G>T
AA Mutation	p.Arg554Ser(p.R554S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265854
Start	2225456:2225456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245G>C
AA Mutation	p.Arg82Pro(p.R82P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265854
Start	1816079:1816079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774776172
CDS Mutation	c.2148C>T
Mutation Classification	Silent
Feature Type	Transcript