Colon Cancer: Gene >> ADAM23

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264377
Start	206560082:206560082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758258908
CDS Mutation	c.1133G>A
AA Mutation	p.Arg378His(p.R378H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264377
Start	206481257:206481257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458T>G
AA Mutation	p.Phe153Cys(p.F153C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264377
Start	206573195:206573195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1737G>T
AA Mutation	p.Gln579His(p.Q579H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264377
Start	206550146:206550146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919A>G
AA Mutation	p.Asn307Asp(p.N307D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264377
Start	206571769:206571769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147866783
CDS Mutation	c.1609G>A
AA Mutation	p.Gly537Arg(p.G537R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264377
Start	206567237:206567237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775680717
CDS Mutation	c.1409G>A
AA Mutation	p.Arg470Gln(p.R470Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264377
Start	206445486:206445486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394C>A
AA Mutation	p.Leu132Ile(p.L132I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264377
Start	206592669:206592669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2011A>G
AA Mutation	p.Ile671Val(p.I671V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264377
Start	206567271:206567271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1443A>T
AA Mutation	p.Arg481Ser(p.R481S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264377
Start	206445371:206445371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264377
Start	206445331:206445331(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.245delA
AA Mutation	p.Asn82IlefsTer87(p.N82Ifs*87)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264377
Start	206596137:206596137(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2340delC
AA Mutation	p.Lys781ArgfsTer14(p.K781Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000264377
Start	206445420:206445420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328G>T
AA Mutation	p.Glu110Ter(p.E110*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000264377
Start	206567221:206567221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1395-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ADAM23

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264377
Start	206481289:206481289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490C>A
AA Mutation	p.Leu164Ile(p.L164I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264377
Start	206594867:206594867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2209C>T
AA Mutation	p.Pro737Ser(p.P737S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264377
Start	206561129:206561129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749823308
CDS Mutation	c.1171C>T
AA Mutation	p.Arg391Trp(p.R391W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript