Colon Cancer: Gene >> DIO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000510508
Start	101561566:101561566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70G>T
AA Mutation	p.Ala24Ser(p.A24S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000510508
Start	101561606:101561606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110G>T
AA Mutation	p.Arg37Met(p.R37M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000510508
Start	101562316:101562316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773838965
CDS Mutation	c.820G>A
AA Mutation	p.Gly274Ser(p.G274S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000510508
Start	101562214:101562214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370365050
CDS Mutation	c.718G>A
AA Mutation	p.Ala240Thr(p.A240T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000510508
Start	101561900:101561900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404C>T
AA Mutation	p.Ala135Val(p.A135V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000510508
Start	101562226:101562226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>A
AA Mutation	p.Asp244Asn(p.D244N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000510508
Start	101562182:101562182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686C>T
AA Mutation	p.Ala229Val(p.A229V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000510508
Start	101562174:101562174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000510508
Start	101561743:101561743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.247G>T
AA Mutation	p.Glu83Ter(p.E83*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000510508
Start	101562193:101562193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.697C>T
AA Mutation	p.Gln233Ter(p.Q233*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DIO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000510508
Start	101562067:101562067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571G>A
AA Mutation	p.Val191Ile(p.V191I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript