Colon Cancer: Gene >> MST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000449682
Start	49684805:49684805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369252300
CDS Mutation	c.1702C>T
AA Mutation	p.Arg568Trp(p.R568W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000449682
Start	49687591:49687591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377644714
CDS Mutation	c.320G>A
AA Mutation	p.Arg107Gln(p.R107Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000449682
Start	49687369:49687369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465T>A
AA Mutation	p.Asp155Glu(p.D155E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000449682
Start	49687469:49687469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745819788
CDS Mutation	c.365G>A
AA Mutation	p.Arg122Gln(p.R122Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000449682
Start	49687648:49687648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263G>A
AA Mutation	p.Ser88Asn(p.S88N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000449682
Start	49686954:49686954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.721C>T
AA Mutation	p.Pro241Ser(p.P241S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000449682
Start	49684571:49684571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1855G>A
AA Mutation	p.Ala619Thr(p.A619T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449682
Start	49687276:49687276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449682
Start	49687608:49687608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189135441
CDS Mutation	c.303G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449682
Start	49687821:49687821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.171C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449682
Start	49684181:49684181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137880382
CDS Mutation	c.2025C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449682
Start	49686321:49686321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000449682
Start	49685484:49685487(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1407_1410delAATC
AA Mutation	p.Ile470TrpfsTer55(p.I470Wfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000449682
Start	49687424:49687424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.410C>T
AA Mutation	p.Ala137Val(p.A137V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449682
Start	49687273:49687273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483T>C
Mutation Classification	Silent
Feature Type	Transcript