Colon Cancer: Gene >> XK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37727858:37727858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.731A>G
AA Mutation	p.Asn244Ser(p.N244S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37694438:37694438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.398G>A
AA Mutation	p.Arg133Gln(p.R133Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37728113:37728113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.986C>T
AA Mutation	p.Ala329Val(p.A329V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37728145:37728145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018A>G
AA Mutation	p.Thr340Ala(p.T340A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37686017:37686017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.56C>G
AA Mutation	p.Thr19Arg(p.T19R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37686008:37686008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781811704
CDS Mutation	c.47C>T
AA Mutation	p.Ala16Val(p.A16V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37727818:37727818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691T>C
AA Mutation	p.Ser231Pro(p.S231P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37728269:37728269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142C>A
AA Mutation	p.Ser381Tyr(p.S381Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37728100:37728100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.973T>G
AA Mutation	p.Phe325Val(p.F325V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378616
Start	37686051:37686051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378616
Start	37694457:37694457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370446008
CDS Mutation	c.417G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378616
Start	37694481:37694481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378616
Start	37694445:37694445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368021749
CDS Mutation	c.405G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378616
Start	37694545:37694545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000378616
Start	37728115:37728116(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.999_1001dupCCT
AA Mutation	p.Leu334dup(p.L334dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> XK

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378616
Start	37728153:37728153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026C>A
Mutation Classification	Silent
Feature Type	Transcript