Colon Cancer: Gene >> ADAM15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356955
Start	155054408:155054408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514C>A
AA Mutation	p.Leu172Ile(p.L172I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356955
Start	155057071:155057071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118C>T
AA Mutation	p.Ala373Val(p.A373V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356955
Start	155058747:155058747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1955T>C
AA Mutation	p.Leu652Pro(p.L652P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356955
Start	155059951:155059951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2045C>T
AA Mutation	p.Pro682Leu(p.P682L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356955
Start	155052702:155052702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111G>T
AA Mutation	p.Glu37Asp(p.E37D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356955
Start	155057100:155057100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147G>A
AA Mutation	p.Asp383Asn(p.D383N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356955
Start	155057957:155057957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1523A>G
AA Mutation	p.Asp508Gly(p.D508G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356955
Start	155058058:155058058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149542900
CDS Mutation	c.1624G>A
AA Mutation	p.Ala542Thr(p.A542T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356955
Start	155061470:155061470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2333C>A
AA Mutation	p.Pro778His(p.P778H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356955
Start	155061972:155061972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759494843
CDS Mutation	c.2421G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356955
Start	155058057:155058057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201800248
CDS Mutation	c.1623C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356955
Start	155057266:155057266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1227C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356955
Start	155061440:155061440(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs779387567
CDS Mutation	c.2309delC
AA Mutation	p.Pro770LeufsTer35(p.P770Lfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ADAM15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356955
Start	155056179:155056179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372429897
CDS Mutation	c.844G>A
AA Mutation	p.Glu282Lys(p.E282K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356955
Start	155056082:155056082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747C>A
AA Mutation	p.Phe249Leu(p.F249L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356955
Start	155058132:155058132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778968775
CDS Mutation	c.1698C>T
Mutation Classification	Silent
Feature Type	Transcript