Colon Cancer: Gene >> ATL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358385
Start	50591554:50591554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437A>G
AA Mutation	p.Asp146Gly(p.D146G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358385
Start	50620658:50620658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773401705
CDS Mutation	c.922G>A
AA Mutation	p.Glu308Lys(p.E308K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358385
Start	50620661:50620661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925A>G
AA Mutation	p.Ser309Gly(p.S309G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358385
Start	50620663:50620663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927C>A
AA Mutation	p.Ser309Arg(p.S309R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358385
Start	50560278:50560278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13C>T
AA Mutation	p.Arg5Cys(p.R5C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358385
Start	50587999:50587999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203T>G
AA Mutation	p.Val68Gly(p.V68G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358385
Start	50587972:50587972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176C>T
AA Mutation	p.Ser59Leu(p.S59L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358385
Start	50632327:50632327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1665G>T
AA Mutation	p.Lys555Asn(p.K555N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000358385
Start	50590941:50590941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Glu95Lys(p.E95K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000358385
Start	50623183:50623183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054G>A
AA Mutation	p.Ala352Thr(p.A352T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358385
Start	50620657:50620657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535790981
CDS Mutation	c.921C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358385
Start	50623234:50623234(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1111delA
AA Mutation	p.Met371TrpfsTer29(p.M371Wfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358385
Start	50620619:50620619(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.887delA
AA Mutation	p.Asn296ThrfsTer2(p.N296Tfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000358385
Start	50628190:50628190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1279G>T
AA Mutation	p.Glu427Ter(p.E427*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000358385
Start	50591010:50591010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754423972
CDS Mutation	c.352C>T
AA Mutation	p.Arg118Ter(p.R118*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ATL1

Mutation ID	1
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000358385
Start	50560297:50560297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.32G>A
AA Mutation	p.Trp11Ter(p.W11*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000358385
Start	50588080:50588080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript