Colon Cancer: Gene >> ADARB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45180408:45180408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1042C>T
AA Mutation	p.Arg348Cys(p.R348C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45220991:45220991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764962336
CDS Mutation	c.2023C>T
AA Mutation	p.Arg675Cys(p.R675C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45176567:45176567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.866C>T
AA Mutation	p.Ala289Val(p.A289V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45176564:45176564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.863C>T
AA Mutation	p.Ala288Val(p.A288V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45222136:45222136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2165C>T
AA Mutation	p.Ala722Val(p.A722V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45183499:45183499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1385C>T
AA Mutation	p.Pro462Leu(p.P462L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45180435:45180435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1069A>G
AA Mutation	p.Met357Val(p.M357V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45204677:45204677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1808G>A
AA Mutation	p.Arg603Gln(p.R603Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45175927:45175927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226C>T
AA Mutation	p.Pro76Ser(p.P76S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45182633:45182633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1127A>C
AA Mutation	p.Lys376Thr(p.K376T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45183472:45183472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358A>T
AA Mutation	p.Asp453Val(p.D453V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45221000:45221000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2032C>T
AA Mutation	p.Arg678Cys(p.R678C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45176314:45176314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613G>A
AA Mutation	p.Asp205Asn(p.D205N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45176258:45176258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755455385
CDS Mutation	c.557C>T
AA Mutation	p.Ala186Val(p.A186V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45176336:45176336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200222908
CDS Mutation	c.635C>T
AA Mutation	p.Pro212Leu(p.P212L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45176432:45176432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774995629
CDS Mutation	c.731G>A
AA Mutation	p.Arg244His(p.R244H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360697
Start	45182685:45182685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360697
Start	45175926:45175926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.225G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360697
Start	45176238:45176238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360697
Start	45176019:45176019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201356458
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ADARB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45182663:45182663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777063481
CDS Mutation	c.1157G>A
AA Mutation	p.Arg386His(p.R386H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45175768:45175768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.67G>T
AA Mutation	p.Asp23Tyr(p.D23Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360697
Start	45176576:45176576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.875C>A
AA Mutation	p.Ala292Asp(p.A292D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360697
Start	45204597:45204597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573950124
CDS Mutation	c.1728C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360697
Start	45182682:45182682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1176C>T
Mutation Classification	Silent
Feature Type	Transcript