Colon Cancer: Gene >> ADAMDEC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256412
Start	24398931:24398931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820G>A
AA Mutation	p.Gly274Arg(p.G274R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256412
Start	24400191:24400191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033G>A
AA Mutation	p.Ala345Thr(p.A345T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000256412
Start	24404087:24404087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1405A>G
AA Mutation	p.Thr469Ala(p.T469A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256412
Start	24397732:24397732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.677T>C
AA Mutation	p.Leu226Pro(p.L226P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256412
Start	24400185:24400185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027A>G
AA Mutation	p.Asn343Asp(p.N343D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000256412
Start	24399009:24399009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.898A>G
AA Mutation	p.Lys300Glu(p.K300E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000256412
Start	24402026:24402026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254G>T
AA Mutation	p.Met418Ile(p.M418I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000256412
Start	24392279:24392279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.106A>G
AA Mutation	p.Thr36Ala(p.T36A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256412
Start	24384555:24384555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754771796
CDS Mutation	c.51C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256412
Start	24400173:24400173(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781693183
CDS Mutation	c.1022delA
AA Mutation	p.Lys341ArgfsTer7(p.K341Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000256412
Start	24397686:24397686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631G>T
AA Mutation	p.Glu211Ter(p.E211*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ADAMDEC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256412
Start	24402077:24402077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1305T>G
AA Mutation	p.Asp435Glu(p.D435E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256412
Start	24398897:24398897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786A>C
AA Mutation	p.Gln262His(p.Q262H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256412
Start	24397721:24397721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.666C>A
Mutation Classification	Silent
Feature Type	Transcript