Colon Cancer: Gene >> TNRC6C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301624
Start	78049562:78049562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500C>A
AA Mutation	p.Ser167Tyr(p.S167Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301624
Start	78051433:78051433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2371C>G
AA Mutation	p.Pro791Ala(p.P791A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301624
Start	78075247:78075247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3029C>A
AA Mutation	p.Ser1010Tyr(p.S1010Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301624
Start	78050225:78050225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1163C>T
AA Mutation	p.Ala388Val(p.A388V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301624
Start	78104819:78104819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5047G>T
AA Mutation	p.Asp1683Tyr(p.D1683Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301624
Start	78051093:78051093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2031T>A
AA Mutation	p.Ser677Arg(p.S677R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301624
Start	78086989:78086989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3698C>T
AA Mutation	p.Ser1233Leu(p.S1233L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000301624
Start	78091539:78091539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3902C>T
AA Mutation	p.Thr1301Met(p.T1301M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301624
Start	78093681:78093681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778067516
CDS Mutation	c.4224C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301624
Start	78086951:78086951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778386206
CDS Mutation	c.3660C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301624
Start	78093705:78093705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4248T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301624
Start	78077298:78077298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3174C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301624
Start	78086972:78086972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3681C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301624
Start	78051291:78051291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2229C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301624
Start	78050433:78050433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1371C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301624
Start	78075161:78075161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370409606
CDS Mutation	c.2943C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301624
Start	78050853:78050853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1791A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301624
Start	78050899:78050899(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs71717398
CDS Mutation	c.1844delA
AA Mutation	p.Asn615MetfsTer45(p.N615Mfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301624
Start	78067919:78067919(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2777delA
AA Mutation	p.Lys926ArgfsTer3(p.K926Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301624
Start	78067906:78067906(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2766delA
AA Mutation	p.Gly923AspfsTer6(p.G923Dfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301624
Start	78051026:78051026(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1969delG
AA Mutation	p.Glu657ArgfsTer3(p.E657Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000301624
Start	78102517:78102517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4545G>A
AA Mutation	p.Trp1515Ter(p.W1515*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301624
Start	78050898:78050899(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1844dupA
AA Mutation	p.Asn615LysfsTer8(p.N615Kfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TNRC6C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301624
Start	78050327:78050327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189050450
CDS Mutation	c.1265G>A
AA Mutation	p.Arg422Gln(p.R422Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301624
Start	78050185:78050185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202206566
CDS Mutation	c.1123G>A
AA Mutation	p.Val375Ile(p.V375I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301624
Start	78049574:78049574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.512C>A
AA Mutation	p.Ser171Tyr(p.S171Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301624
Start	78071093:78071093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2787G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301624
Start	78093093:78093093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4131C>A
Mutation Classification	Silent
Feature Type	Transcript