Colon Cancer: Gene >> THRB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24122922:24122922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348C>A
AA Mutation	p.Leu450Ile(p.L450I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24123120:24123120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1150C>T
AA Mutation	p.Pro384Ser(p.P384S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24127694:24127694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121918690
CDS Mutation	c.949G>A
AA Mutation	p.Ala317Thr(p.A317T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24143575:24143575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664A>G
AA Mutation	p.Ile222Val(p.I222V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24190220:24190220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556429294
CDS Mutation	c.137G>A
AA Mutation	p.Arg46His(p.R46H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24122889:24122889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1381G>T
AA Mutation	p.Asp461Tyr(p.D461Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24190193:24190193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164C>T
AA Mutation	p.Ser55Leu(p.S55L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24146710:24146710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.497T>A
AA Mutation	p.Phe166Tyr(p.F166Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24123016:24123016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254G>C
AA Mutation	p.Trp418Cys(p.W418C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24143547:24143547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768167319
CDS Mutation	c.692C>T
AA Mutation	p.Ala231Val(p.A231V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24127526:24127526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1117C>T
AA Mutation	p.Leu373Phe(p.L373F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24190260:24190260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97T>C
AA Mutation	p.Ser33Pro(p.S33P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24146771:24146771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.436A>G
AA Mutation	p.Lys146Glu(p.K146E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356447
Start	24143600:24143600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371602445
CDS Mutation	c.639G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356447
Start	24143591:24143591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143993214
CDS Mutation	c.648C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356447
Start	24190306:24190306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.51G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356447
Start	24146773:24146773(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.434delG
AA Mutation	p.Cys145LeufsTer9(p.C145Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000356447
Start	24123016:24123016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254G>A
AA Mutation	p.Trp418Ter(p.W418*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> THRB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356447
Start	24190193:24190193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164C>T
AA Mutation	p.Ser55Leu(p.S55L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript