Colon Cancer: Gene >> ALPL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374832
Start	21577599:21577599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs79250591
CDS Mutation	c.1526G>A
AA Mutation	p.Gly509Asp(p.G509D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374832
Start	21576524:21576524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1192C>A
AA Mutation	p.Leu398Met(p.L398M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374832
Start	21575855:21575855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552831415
CDS Mutation	c.1120G>A
AA Mutation	p.Val374Met(p.V374M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374832
Start	21563266:21563266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200621180
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Cys(p.R152C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374832
Start	21563224:21563224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748874853
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Trp(p.R138W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374832
Start	21570327:21570327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781272386
CDS Mutation	c.815G>A
AA Mutation	p.Arg272His(p.R272H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374832
Start	21577421:21577421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138690664
CDS Mutation	c.1348C>T
AA Mutation	p.Arg450Cys(p.R450C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374832
Start	21560653:21560653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753550135
CDS Mutation	c.89G>A
AA Mutation	p.Arg30Gln(p.R30Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374832
Start	21577489:21577489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369433931
CDS Mutation	c.1416C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374832
Start	21563205:21563205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374832
Start	21563193:21563193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368714904
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374832
Start	21577555:21577555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142545037
CDS Mutation	c.1482C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374832
Start	21560663:21560663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772424729
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374832
Start	21575901:21575901(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs779683021
CDS Mutation	c.1171delC
AA Mutation	p.Arg391ValfsTer12(p.R391Vfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374832
Start	21568112:21568112(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769948289
CDS Mutation	c.662delG
AA Mutation	p.Gly221ValfsTer56(p.G221Vfs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ALPL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374832
Start	21577490:21577490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1417G>A
AA Mutation	p.Gly473Ser(p.G473S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374832
Start	21560663:21560663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772424729
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript