Colon Cancer: Gene >> HADHB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317799
Start	26283041:26283041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1051C>A
AA Mutation	p.Leu351Ile(p.L351I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317799
Start	26289931:26289931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1403T>A
AA Mutation	p.Ile468Lys(p.I468K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317799
Start	26278773:26278773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.602A>C
AA Mutation	p.Lys201Thr(p.K201T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317799
Start	26254463:26254463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372980146
CDS Mutation	c.98G>A
AA Mutation	p.Arg33Gln(p.R33Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317799
Start	26254313:26254313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.59G>T
AA Mutation	p.Arg20Ile(p.R20I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317799
Start	26278676:26278676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505T>C
AA Mutation	p.Ser169Pro(p.S169P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000317799
Start	26278779:26278779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749861331
CDS Mutation	c.608G>A
AA Mutation	p.Arg203Gln(p.R203Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000317799
Start	26263454:26263454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768738452
CDS Mutation	c.184A>G
AA Mutation	p.Thr62Ala(p.T62A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000317799
Start	26278778:26278778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534616210
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Ter(p.R203*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HADHB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317799
Start	26273695:26273695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299A>G
AA Mutation	p.Tyr100Cys(p.Y100C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317799
Start	26280056:26280056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874C>G
AA Mutation	p.Leu292Val(p.L292V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317799
Start	26263396:26263396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126G>A
Mutation Classification	Silent
Feature Type	Transcript