Colon Cancer: Gene >> RPS6KA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262752
Start	84107037:84107037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1115C>A
AA Mutation	p.Ser372Tyr(p.S372Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262752
Start	84104566:84104566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1547C>T
AA Mutation	p.Ser516Leu(p.S516L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262752
Start	84187889:84187889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11T>C
AA Mutation	p.Phe4Ser(p.F4S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262752
Start	84107023:84107023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1129G>T
AA Mutation	p.Ala377Ser(p.A377S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262752
Start	84065019:84065019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2064G>C
AA Mutation	p.Gln688His(p.Q688H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262752
Start	84096258:84096258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1907G>T
AA Mutation	p.Arg636Leu(p.R636L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262752
Start	84104582:84104582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1531A>G
AA Mutation	p.Lys511Glu(p.K511E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262752
Start	84156154:84156154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.179A>G
AA Mutation	p.His60Arg(p.H60R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262752
Start	84117065:84117065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944G>A
AA Mutation	p.Arg315Lys(p.R315K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262752
Start	84102092:84102092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1721G>T
AA Mutation	p.Gly574Val(p.G574V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262752
Start	84106431:84106431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1299T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262752
Start	84106371:84106371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1359A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262752
Start	84096257:84096257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1908T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262752
Start	84096215:84096215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1950C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262752
Start	84148055:84148055(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs756096568
CDS Mutation	c.327delA
AA Mutation	p.Ala110ProfsTer3(p.A110Pfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000262752
Start	84102074:84102074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1739T>A
AA Mutation	p.Leu580Ter(p.L580*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262752
Start	84116246:84116247(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.990dupT
AA Mutation	p.Ala331CysfsTer4(p.A331Cfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262752
Start	84107631:84107632(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1102dupA
AA Mutation	p.Thr368AsnfsTer3(p.T368Nfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262752
Start	84148054:84148055(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.327dupA
AA Mutation	p.Ala110SerfsTer36(p.A110Sfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262752
Start	84102102:84102103(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1710_1711insTT
AA Mutation	p.Gln571PhefsTer11(p.Q571Ffs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262752
Start	84148064:84148065(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.317_318insAATATTACCTACAG
AA Mutation	p.Leu107IlefsTer6(p.L107Ifs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262752
Start	84148066:84148067(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.315_316insATCAAATCTA
AA Mutation	p.Val106IlefsTer43(p.V106Ifs*43)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	inframe_insertion;splice_region_variant
Transcription ID	ENST00000262752
Start	84065109:84065110(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1973_1974insCATAAAAGTATG
AA Mutation	p.Asp658_Leu659insIleLysValCys(p.D658_L659insIKVC)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RPS6KA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262752
Start	84106971:84106971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1181C>T
AA Mutation	p.Ser394Phe(p.S394F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000262752
Start	84134787:84134787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641T>A
AA Mutation	p.Leu214Ter(p.L214*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript