Colon Cancer: Gene >> A1CF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373993
Start	50859890:50859890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754321707
CDS Mutation	c.51A>C
AA Mutation	p.Glu17Asp(p.E17D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373993
Start	50813865:50813865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190691295
CDS Mutation	c.1339G>A
AA Mutation	p.Ala447Thr(p.A447T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373993
Start	50813922:50813922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282G>A
AA Mutation	p.Gly428Arg(p.G428R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373993
Start	50809981:50809981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765124661
CDS Mutation	c.1546G>A
AA Mutation	p.Glu516Lys(p.E516K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373993
Start	50841989:50841989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.238G>A
AA Mutation	p.Gly80Ser(p.G80S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373993
Start	50809940:50809940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777970091
CDS Mutation	c.1587C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373993
Start	50806852:50806852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1662C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373993
Start	50836216:50836216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76706180
CDS Mutation	c.462G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373993
Start	50816109:50816109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373993
Start	50859857:50859857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.84A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000373993
Start	50820623:50820623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772118222
CDS Mutation	c.796C>T
AA Mutation	p.Arg266Ter(p.R266*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000373993
Start	50836227:50836227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451G>T
AA Mutation	p.Glu151Ter(p.E151*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000373993
Start	50811140:50811140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1384C>T
AA Mutation	p.Gln462Ter(p.Q462*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373993
Start	50814027:50814028(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1176_1177insT
AA Mutation	p.Val393CysfsTer32(p.V393Cfs*32)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373993
Start	50814028:50814029(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1175_1176insTTTTA
AA Mutation	p.Val393PhefsTer3(p.V393Ffs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> A1CF

Mutation ID	1
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000373993
Start	50809900:50809901(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1618_1626dupGCTACTGCT
AA Mutation	p.Ala540_Ala542dup(p.A540_A542dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript