Colon Cancer: Gene >> FOXG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28768698:28768698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1419T>G
AA Mutation	p.Asp473Glu(p.D473E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28768457:28768457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1178C>T
AA Mutation	p.Ser393Leu(p.S393L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28768540:28768540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1261G>A
AA Mutation	p.Val421Ile(p.V421I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28768124:28768124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.845C>T
AA Mutation	p.Ala282Val(p.A282V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28768595:28768595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770118439
CDS Mutation	c.1316C>T
AA Mutation	p.Ala439Val(p.A439V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28767827:28767827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548C>T
AA Mutation	p.Pro183Leu(p.P183L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28768069:28768069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790G>A
AA Mutation	p.Val264Met(p.V264M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28768099:28768099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820C>T
AA Mutation	p.Arg274Trp(p.R274W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28768022:28768022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.743A>G
AA Mutation	p.Asp248Gly(p.D248G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28767383:28767383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104C>T
AA Mutation	p.Ala35Val(p.A35V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28767839:28767839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.560A>C
AA Mutation	p.Asn187Thr(p.N187T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28767968:28767968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs786205007
CDS Mutation	c.689G>A
AA Mutation	p.Arg230His(p.R230H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28768426:28768426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202157686
CDS Mutation	c.1147G>A
AA Mutation	p.Ala383Thr(p.A383T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28767763:28767763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484G>T
AA Mutation	p.Gly162Cys(p.G162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28767937:28767937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658G>A
AA Mutation	p.Glu220Lys(p.E220K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28768509:28768509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1230C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28768008:28768008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.729G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28767381:28767381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.102C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28767318:28767318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.39C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28768506:28768506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1227G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28768563:28768563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1284G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28768263:28768263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774246700
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28768299:28768299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1020C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28767933:28767933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28768614:28768614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1335G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28767840:28767840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28768653:28768653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1374C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FOXG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28768282:28768282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531378284
CDS Mutation	c.1003C>G
AA Mutation	p.Pro335Ala(p.P335A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313071
Start	28767904:28767904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625G>A
AA Mutation	p.Glu209Lys(p.E209K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313071
Start	28767948:28767948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000313071
Start	28768281:28768281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1002C>A
AA Mutation	p.Tyr334Ter(p.Y334*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript