Colon Cancer: Gene >> ABCG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361802
Start	42225882:42225882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781254615
CDS Mutation	c.254C>T
AA Mutation	p.Ser85Leu(p.S85L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361802
Start	42282350:42282350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.665G>A
AA Mutation	p.Arg222His(p.R222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361802
Start	42291656:42291656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1689G>T
AA Mutation	p.Gln563His(p.Q563H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361802
Start	42288311:42288311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756708334
CDS Mutation	c.1259C>T
AA Mutation	p.Ser420Leu(p.S420L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361802
Start	42273356:42273356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.458G>A
AA Mutation	p.Arg153His(p.R153H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361802
Start	42287894:42287894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979G>A
AA Mutation	p.Glu327Lys(p.E327K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361802
Start	42296342:42296342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1987C>T
AA Mutation	p.Arg663Cys(p.R663C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361802
Start	42282356:42282356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671G>A
AA Mutation	p.Arg224His(p.R224H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361802
Start	42296173:42296173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1818C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361802
Start	42291524:42291524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559616836
CDS Mutation	c.1557C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361802
Start	42284668:42284668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368376675
CDS Mutation	c.843C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361802
Start	42287948:42287948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000361802
Start	42296304:42296305(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1949_1950insAGGAGGAAA
AA Mutation	p.Leu650_Asp651insGlyGlyLys(p.L650_D651insGGK)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ABCG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361802
Start	42282402:42282402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717C>A
AA Mutation	p.Phe239Leu(p.F239L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361802
Start	42294589:42294589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1737C>A
AA Mutation	p.Phe579Leu(p.F579L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361802
Start	42291551:42291551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374817134
CDS Mutation	c.1584G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361802
Start	42296173:42296173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1818C>T
Mutation Classification	Silent
Feature Type	Transcript