Colon Cancer: Gene >> DNMT3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264709
Start	25246204:25246204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200845575
CDS Mutation	c.1385C>T
AA Mutation	p.Ala462Val(p.A462V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264709
Start	25248051:25248051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>A
AA Mutation	p.Glu281Lys(p.E281K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264709
Start	25240417:25240417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139293773
CDS Mutation	c.2207G>A
AA Mutation	p.Arg736His(p.R736H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264709
Start	25313974:25313974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11T>C
AA Mutation	p.Met4Thr(p.M4T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264709
Start	25240655:25240655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2158C>T
AA Mutation	p.Arg720Cys(p.R720C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264709
Start	25300179:25300179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137G>A
AA Mutation	p.Arg46Gln(p.R46Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264709
Start	25234346:25234346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2672G>A
AA Mutation	p.Arg891Gln(p.R891Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264709
Start	25282615:25282615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274G>A
AA Mutation	p.Asp92Asn(p.D92N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264709
Start	25246050:25246050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444G>A
AA Mutation	p.Glu482Lys(p.E482K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264709
Start	25275005:25275005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575C>T
AA Mutation	p.Ala192Val(p.A192V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264709
Start	25240344:25240344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2280C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264709
Start	25248139:25248139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264709
Start	25246720:25246720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264709
Start	25234305:25234305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2713C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264709
Start	25239141:25239141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2397C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264709
Start	25313970:25313970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.15C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264709
Start	25247693:25247693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.912C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DNMT3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264709
Start	25274954:25274954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626G>A
AA Mutation	p.Arg209His(p.R209H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264709
Start	25236949:25236949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2465G>A
AA Mutation	p.Gly822Asp(p.G822D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264709
Start	25235799:25235799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138445723
CDS Mutation	c.2505G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264709
Start	25244632:25244632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771486108
CDS Mutation	c.1575G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000264709
Start	25239188:25239188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2350G>T
AA Mutation	p.Glu784Ter(p.E784*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript