Colon Cancer: Gene >> HGS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329138
Start	81685674:81685674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770624508
CDS Mutation	c.107G>A
AA Mutation	p.Arg36His(p.R36H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329138
Start	81700550:81700550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766795726
CDS Mutation	c.1966G>A
AA Mutation	p.Ala656Thr(p.A656T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329138
Start	81694833:81694833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.955G>A
AA Mutation	p.Ala319Thr(p.A319T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329138
Start	81691466:81691466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557G>A
AA Mutation	p.Gly186Glu(p.G186E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329138
Start	81688759:81688759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.347C>T
AA Mutation	p.Ala116Val(p.A116V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329138
Start	81684100:81684100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34C>A
AA Mutation	p.Leu12Ile(p.L12I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000329138
Start	81701589:81701589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2305A>G
AA Mutation	p.Ser769Gly(p.S769G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000329138
Start	81700512:81700512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201755663
CDS Mutation	c.1928G>T
AA Mutation	p.Gly643Val(p.G643V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329138
Start	81701107:81701107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140803494
CDS Mutation	c.2199G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329138
Start	81685672:81685672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329138
Start	81687059:81687059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329138
Start	81686366:81686366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329138
Start	81693540:81693540(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.705delC
AA Mutation	p.Glu236SerfsTer3(p.E236Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HGS

No Mutation Annotation!