Colon Cancer: Gene >> OPLAH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144054681:144054681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2566C>G
AA Mutation	p.His856Asp(p.H856D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144056704:144056704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1758C>A
AA Mutation	p.Asp586Glu(p.D586E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144056429:144056429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371821782
CDS Mutation	c.1939G>A
AA Mutation	p.Glu647Lys(p.E647K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144059888:144059888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782616822
CDS Mutation	c.145G>A
AA Mutation	p.Glu49Lys(p.E49K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144055875:144055875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782158791
CDS Mutation	c.2161G>A
AA Mutation	p.Val721Met(p.V721M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144055875:144055875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782158791
CDS Mutation	c.2161G>T
AA Mutation	p.Val721Leu(p.V721L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144058254:144058254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934G>A
AA Mutation	p.Gly312Ser(p.G312S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144056674:144056674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1788C>A
AA Mutation	p.His596Gln(p.H596Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144056150:144056150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2093A>G
AA Mutation	p.Asn698Ser(p.N698S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144058668:144058668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611T>C
AA Mutation	p.Val204Ala(p.V204A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144059031:144059031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412G>A
AA Mutation	p.Glu138Lys(p.E138K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144052564:144052564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3188G>A
AA Mutation	p.Arg1063Gln(p.R1063Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144053316:144053316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2764G>T
AA Mutation	p.Asp922Tyr(p.D922Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144053039:144053039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2962G>T
AA Mutation	p.Asp988Tyr(p.D988Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144058367:144058367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.821T>C
AA Mutation	p.Leu274Pro(p.L274P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144052211:144052211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3419T>C
AA Mutation	p.Met1140Thr(p.M1140T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144059657:144059657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.305G>A
AA Mutation	p.Arg102His(p.R102H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000618853
Start	144057250:144057250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1493C>T
AA Mutation	p.Ala498Val(p.A498V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618853
Start	144056397:144056397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1971C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618853
Start	144052237:144052237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3393C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618853
Start	144058781:144058781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.579C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000618853
Start	144054639:144054639(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781956288
CDS Mutation	c.2608delC
AA Mutation	p.His870ThrfsTer28(p.H870Tfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000618853
Start	144055076:144055076(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2362delC
AA Mutation	p.His788ThrfsTer31(p.H788Tfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> OPLAH

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000618853
Start	144054639:144054639(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781956288
CDS Mutation	c.2608delC
AA Mutation	p.His870ThrfsTer28(p.H870Tfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript