Colon Cancer: Gene >> TBX18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84744318:84744318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947G>A
AA Mutation	p.Arg316His(p.R316H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84736751:84736751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1758C>A
AA Mutation	p.Phe586Leu(p.F586L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000369663
Start	84762544:84762544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.497G>A
AA Mutation	p.Arg166Lys(p.R166K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84737201:84737201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1308G>T
AA Mutation	p.Glu436Asp(p.E436D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84748051:84748051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.808G>A
AA Mutation	p.Val270Met(p.V270M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84737343:84737343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166T>C
AA Mutation	p.Leu389Pro(p.L389P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84748071:84748071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.788T>C
AA Mutation	p.Met263Thr(p.M263T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84748056:84748056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372776015
CDS Mutation	c.803C>T
AA Mutation	p.Pro268Leu(p.P268L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84738539:84738539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571410094
CDS Mutation	c.1057C>T
AA Mutation	p.Arg353Trp(p.R353W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84762622:84762622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419G>A
AA Mutation	p.Arg140Gln(p.R140Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84756723:84756723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746A>G
AA Mutation	p.Asn249Ser(p.N249S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000369663
Start	84760355:84760355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499C>T
AA Mutation	p.Arg167Cys(p.R167C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84744268:84744268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997C>T
AA Mutation	p.Arg333Cys(p.R333C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84764052:84764052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130G>A
AA Mutation	p.Glu44Lys(p.E44K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84763995:84763995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187G>A
AA Mutation	p.Glu63Lys(p.E63K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369663
Start	84736718:84736718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1791G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369663
Start	84756851:84756851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150088516
CDS Mutation	c.618G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369663
Start	84747992:84747992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771393702
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369663
Start	84762624:84762624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369663
Start	84748055:84748055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755758645
CDS Mutation	c.804G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369663
Start	84764113:84764113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.69G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369663
Start	84756743:84756743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148004775
CDS Mutation	c.726C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369663
Start	84736895:84736895(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1614delC
AA Mutation	p.Lys539AsnfsTer25(p.K539Nfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TBX18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84756864:84756864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605T>C
AA Mutation	p.Val202Ala(p.V202A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369663
Start	84756852:84756852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617C>T
AA Mutation	p.Ser206Leu(p.S206L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000369663
Start	84748088:84748088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript