Colon Cancer: Gene >> ADAM10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260408
Start	58633206:58633206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166T>G
AA Mutation	p.Phe389Cys(p.F389C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260408
Start	58627858:58627858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202C>T
AA Mutation	p.Pro401Leu(p.P401L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260408
Start	58627774:58627774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286A>G
AA Mutation	p.Asn429Ser(p.N429S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260408
Start	58621509:58621509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1473G>T
AA Mutation	p.Glu491Asp(p.E491D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260408
Start	58646074:58646074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752797397
CDS Mutation	c.716G>A
AA Mutation	p.Arg239Gln(p.R239Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260408
Start	58640906:58640906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883A>G
AA Mutation	p.Ile295Val(p.I295V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260408
Start	58643935:58643935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779C>T
AA Mutation	p.Thr260Ile(p.T260I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000260408
Start	58643904:58643904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810C>A
AA Mutation	p.Phe270Leu(p.F270L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260408
Start	58627725:58627725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1335G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260408
Start	58640811:58640811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772080878
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260408
Start	58633202:58633202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1170A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260408
Start	58597628:58597628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2166G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260408
Start	58610430:58610430(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1892delC
AA Mutation	p.Pro631LeufsTer17(p.P631Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ADAM10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260408
Start	58599672:58599672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2078C>T
AA Mutation	p.Ala693Val(p.A693V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260408
Start	58633325:58633325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1047C>A
Mutation Classification	Silent
Feature Type	Transcript