Colon Cancer: Gene >> GATA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376670
Start	48792403:48792403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679G>A
AA Mutation	p.Ala227Thr(p.A227T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376670
Start	48791282:48791282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782299679
CDS Mutation	c.173C>T
AA Mutation	p.Ala58Val(p.A58V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376670
Start	48794013:48794013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1091A>G
AA Mutation	p.Tyr364Cys(p.Y364C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376670
Start	48792072:48792072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449C>A
AA Mutation	p.Pro150His(p.P150H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376670
Start	48791980:48791980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.357G>T
AA Mutation	p.Gln119His(p.Q119H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376670
Start	48793952:48793952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141479621
CDS Mutation	c.1030G>A
AA Mutation	p.Gly344Arg(p.G344R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376670
Start	48791923:48791923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300G>T
AA Mutation	p.Lys100Asn(p.K100N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376670
Start	48792194:48792194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140561920
CDS Mutation	c.571C>T
AA Mutation	p.Arg191Cys(p.R191C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376670
Start	48792447:48792447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376670
Start	48793990:48793990(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1073delC
AA Mutation	p.Pro358GlnfsTer74(p.P358Qfs*74)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376670
Start	48794119:48794120(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1203dupC
AA Mutation	p.Thr402HisfsTer48(p.T402Hfs*48)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GATA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376670
Start	48794018:48794018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096G>T
AA Mutation	p.Gly366Cys(p.G366C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript