Colon Cancer: Gene >> TFAP2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000482890
Start	10404556:10404556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.716C>T
AA Mutation	p.Ser239Leu(p.S239L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000482890
Start	10400548:10400548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756122879
CDS Mutation	c.925G>A
AA Mutation	p.Glu309Lys(p.E309K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000482890
Start	10398530:10398530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201T>C
AA Mutation	p.Tyr401His(p.Y401H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000482890
Start	10410259:10410259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122G>T
AA Mutation	p.Ser41Ile(p.S41I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000482890
Start	10409995:10409995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.386G>A
AA Mutation	p.Arg129Gln(p.R129Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000482890
Start	10414969:10414969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.17C>T
AA Mutation	p.Thr6Met(p.T6M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000482890
Start	10400542:10400542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931G>A
AA Mutation	p.Glu311Lys(p.E311K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000482890
Start	10410096:10410096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000482890
Start	10404642:10404642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000482890
Start	10406830:10406830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.495G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000482890
Start	10400512:10400513(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.960_961insTGTTTCTCTTT
AA Mutation	p.Leu321CysfsTer16(p.L321Cfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TFAP2A

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000482890
Start	10402607:10402607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768G>A
Mutation Classification	Silent
Feature Type	Transcript