Colon Cancer: Gene >> RNF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214521:26214521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1361G>A
AA Mutation	p.Arg454Gln(p.R454Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26215022:26215022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860G>T
AA Mutation	p.Ser287Ile(p.S287I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26218554:26218554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246A>C
AA Mutation	p.Gln82His(p.Q82H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26215404:26215404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478A>G
AA Mutation	p.Arg160Gly(p.R160G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26215419:26215419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763605133
CDS Mutation	c.463G>A
AA Mutation	p.Val155Ile(p.V155I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214602:26214602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1280T>C
AA Mutation	p.Leu427Pro(p.L427P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26215128:26215128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754C>T
AA Mutation	p.Arg252Cys(p.R252C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214077:26214077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368287151
CDS Mutation	c.1805G>A
AA Mutation	p.Arg602Gln(p.R602Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214795:26214795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087G>A
AA Mutation	p.Ala363Thr(p.A363T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214992:26214992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.890G>T
AA Mutation	p.Arg297Ile(p.R297I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214971:26214971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776378212
CDS Mutation	c.911G>A
AA Mutation	p.Arg304Gln(p.R304Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26215440:26215440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Trp(p.R148W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346166
Start	26214943:26214943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.939A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346166
Start	26214544:26214544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1338T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346166
Start	26213950:26213950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754717341
CDS Mutation	c.1932G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346166
Start	26214520:26214520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1362A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346166
Start	26214104:26214104(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1778delT
AA Mutation	p.Leu593TyrfsTer2(p.L593Yfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346166
Start	26213839:26213840(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2042_2043delTA
AA Mutation	p.Ile681SerfsTer7(p.I681Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000346166
Start	26214096:26214096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1786G>T
AA Mutation	p.Glu596Ter(p.E596*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000346166
Start	26214972:26214972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.910C>T
AA Mutation	p.Arg304Ter(p.R304*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000346166
Start	26214705:26214705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762149904
CDS Mutation	c.1177C>T
AA Mutation	p.Arg393Ter(p.R393*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346166
Start	26214103:26214104(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1778dupT
AA Mutation	p.Leu593PhefsTer4(p.L593Ffs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346166
Start	26215397:26215398(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.484_485insGGAACTACTACCA
AA Mutation	p.Phe162TrpfsTer6(p.F162Wfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RNF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214293:26214293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1589G>T
AA Mutation	p.Ser530Ile(p.S530I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214044:26214044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1838A>C
AA Mutation	p.Asn613Thr(p.N613T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214923:26214923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.959G>A
AA Mutation	p.Gly320Asp(p.G320D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000346166
Start	26214624:26214624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1258A>T
AA Mutation	p.Arg420Ter(p.R420*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346166
Start	26214103:26214104(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1778dupT
AA Mutation	p.Leu593PhefsTer4(p.L593Ffs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript