Colon Cancer: Gene >> WASF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359451
Start	110113446:110113446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148G>T
AA Mutation	p.Asp50Tyr(p.D50Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359451
Start	110101720:110101720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390G>T
AA Mutation	p.Gly464Cys(p.G464C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359451
Start	110102066:110102066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359451
Start	110102126:110102126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359451
Start	110102135:110102136(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.974dupC
AA Mutation	p.Pro326ThrfsTer77(p.P326Tfs*77)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359451
Start	110105527:110105528(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.592_593insTTGTTTCAAA
AA Mutation	p.His198LeufsTer5(p.H198Lfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000359451
Start	110103558:110103558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> WASF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359451
Start	110102208:110102208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902C>T
AA Mutation	p.Thr301Ile(p.T301I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359451
Start	110108645:110108645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305G>A
AA Mutation	p.Arg102Gln(p.R102Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359451
Start	110108613:110108613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752451504
CDS Mutation	c.337G>A
AA Mutation	p.Asp113Asn(p.D113N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359451
Start	110100565:110100565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377750682
CDS Mutation	c.1637C>T
AA Mutation	p.Ser546Leu(p.S546L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359451
Start	110113420:110113420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.174A>G
Mutation Classification	Silent
Feature Type	Transcript