Colon Cancer: Gene >> CASP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310447
Start	143292687:143292687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144817015
CDS Mutation	c.464G>A
AA Mutation	p.Arg155His(p.R155H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310447
Start	143304962:143304962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250G>A
AA Mutation	p.Arg417Gln(p.R417Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310447
Start	143300234:143300234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756201685
CDS Mutation	c.907G>A
AA Mutation	p.Ala303Thr(p.A303T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310447
Start	143299989:143299989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370097426
CDS Mutation	c.814G>A
AA Mutation	p.Val272Met(p.V272M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310447
Start	143294744:143294744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141615673
CDS Mutation	c.718G>A
AA Mutation	p.Val240Ile(p.V240I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000310447
Start	143299925:143299925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.750A>C
AA Mutation	p.Glu250Asp(p.E250D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310447
Start	143304685:143304685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129A>G
AA Mutation	p.Met377Val(p.M377V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000310447
Start	143299934:143299934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.759G>T
AA Mutation	p.Glu253Asp(p.E253D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310447
Start	143304681:143304681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1125C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310447
Start	143294294:143294294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759397296
CDS Mutation	c.540T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310447
Start	143303878:143303878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561597102
CDS Mutation	c.1062G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000310447
Start	143294770:143294771(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.744_745insACCTATATG
AA Mutation	p.Ala248_Gln249insThrTyrMet(p.A248_Q249insTYM)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CASP2

No Mutation Annotation!