Colon Cancer: Gene >> ADAMTS6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65226174:65226174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1979A>C
AA Mutation	p.Asn660Thr(p.N660T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381055
Start	65242206:65242206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1831C>T
AA Mutation	p.Pro611Ser(p.P611S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65197130:65197130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2597T>C
AA Mutation	p.Val866Ala(p.V866A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65452747:65452747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803G>A
AA Mutation	p.Arg268His(p.R268H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65471010:65471010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230A>T
AA Mutation	p.Asp77Val(p.D77V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65170676:65170676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3185C>T
AA Mutation	p.Pro1062Leu(p.P1062L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65260604:65260604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1826C>T
AA Mutation	p.Thr609Ile(p.T609I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65188116:65188116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2810C>T
AA Mutation	p.Thr937Met(p.T937M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65226160:65226160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1993C>T
AA Mutation	p.Arg665Cys(p.R665C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65226201:65226201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1952C>T
AA Mutation	p.Ala651Val(p.A651V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65452742:65452742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808G>T
AA Mutation	p.Asp270Tyr(p.D270Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381055
Start	65300044:65300044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1311G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381055
Start	65151905:65151905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3285G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381055
Start	65260660:65260660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1770T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381055
Start	65170633:65170633(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3228delC
AA Mutation	p.Ile1077PhefsTer10(p.I1077Ffs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381055
Start	65188073:65188073(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2853delA
AA Mutation	p.Glu952SerfsTer89(p.E952Sfs*89)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381055
Start	65188206:65188207(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2719dupG
AA Mutation	p.Asp907GlyfsTer10(p.D907Gfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ADAMTS6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65470885:65470885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>T
AA Mutation	p.Asp119Tyr(p.D119Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65215449:65215449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2311G>C
AA Mutation	p.Ala771Pro(p.A771P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65224951:65224951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2164T>C
AA Mutation	p.Phe722Leu(p.F722L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381055
Start	65329435:65329435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1166T>C
AA Mutation	p.Ile389Thr(p.I389T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381055
Start	65170680:65170680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3181C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381055
Start	65188079:65188079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778331507
CDS Mutation	c.2847C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381055
Start	65215479:65215480(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2280dupA
AA Mutation	p.Ser761IlefsTer2(p.S761Ifs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript