Colon Cancer: Gene >> ABCG8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43846249:43846249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260G>A
AA Mutation	p.Gly87Asp(p.G87D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43875305:43875305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149441561
CDS Mutation	c.1648G>A
AA Mutation	p.Ala550Thr(p.A550T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43877620:43877620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1816A>G
AA Mutation	p.Ile606Val(p.I606V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43852764:43852764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201133496
CDS Mutation	c.860C>T
AA Mutation	p.Thr287Met(p.T287M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43875257:43875257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1600C>A
AA Mutation	p.Leu534Met(p.L534M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43852435:43852435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643G>A
AA Mutation	p.Gly215Arg(p.G215R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43877842:43877842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1951A>G
AA Mutation	p.Ser651Gly(p.S651G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43839096:43839096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761344788
CDS Mutation	c.43G>A
AA Mutation	p.Ala15Thr(p.A15T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43873923:43873923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754133516
CDS Mutation	c.1348G>A
AA Mutation	p.Ala450Thr(p.A450T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43875396:43875396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1739T>C
AA Mutation	p.Leu580Ser(p.L580S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43851812:43851812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766212636
CDS Mutation	c.551G>A
AA Mutation	p.Arg184His(p.R184H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43846202:43846202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.213C>G
AA Mutation	p.Phe71Leu(p.F71L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43877636:43877636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1832G>A
AA Mutation	p.Arg611Lys(p.R611K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43851715:43851715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762452685
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Cys(p.R152C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272286
Start	43872118:43872118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272286
Start	43873817:43873817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1242G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ABCG8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43852403:43852403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144730815
CDS Mutation	c.611G>A
AA Mutation	p.Arg204His(p.R204H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43851715:43851715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762452685
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Cys(p.R152C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43852616:43852616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34754243
CDS Mutation	c.712G>A
AA Mutation	p.Glu238Lys(p.E238K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272286
Start	43877636:43877636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1832G>T
AA Mutation	p.Arg611Ile(p.R611I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript