Colon Cancer: Gene >> ABCC10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43438725:43438725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2057T>G
AA Mutation	p.Phe686Cys(p.F686C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43449149:43449149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4148C>A
AA Mutation	p.Ser1383Tyr(p.S1383Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43435776:43435776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368489601
CDS Mutation	c.1634G>A
AA Mutation	p.Arg545Gln(p.R545Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43441946:43441946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2212C>T
AA Mutation	p.Arg738Cys(p.R738C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43449476:43449476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4258C>T
AA Mutation	p.Leu1420Phe(p.L1420F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43449431:43449431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4213A>G
AA Mutation	p.Ile1405Val(p.I1405V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43447825:43447825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3847G>T
AA Mutation	p.Gly1283Cys(p.G1283C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43450002:43450002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4390G>A
AA Mutation	p.Ala1464Thr(p.A1464T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43434745:43434745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1505T>C
AA Mutation	p.Leu502Pro(p.L502P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43432186:43432186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750724181
CDS Mutation	c.206G>A
AA Mutation	p.Arg69Gln(p.R69Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000372530
Start	43435907:43435907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1765G>T
AA Mutation	p.Asp589Tyr(p.D589Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43445752:43445752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3184T>C
AA Mutation	p.Ser1062Pro(p.S1062P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43444863:43444863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748925933
CDS Mutation	c.2765C>T
AA Mutation	p.Ala922Val(p.A922V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372530
Start	43449526:43449526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4308T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372530
Start	43432778:43432778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.798C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372530
Start	43433249:43433249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776357831
CDS Mutation	c.1269C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372530
Start	43438647:43438647(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1983delG
AA Mutation	p.Leu662CysfsTer38(p.L662Cfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372530
Start	43435885:43435885(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1747delC
AA Mutation	p.Gln583ArgfsTer41(p.Q583Rfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000372530
Start	43432185:43432185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142310490
CDS Mutation	c.205C>T
AA Mutation	p.Arg69Ter(p.R69*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ABCC10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43433113:43433113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1133G>A
AA Mutation	p.Gly378Glu(p.G378E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372530
Start	43432684:43432684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200394501
CDS Mutation	c.704G>A
AA Mutation	p.Arg235His(p.R235H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript