Colon Cancer: Gene >> ASIC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359872
Start	33017625:33017625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348C>T
AA Mutation	p.Leu450Phe(p.L450F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359872
Start	33088984:33088984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147403420
CDS Mutation	c.713C>T
AA Mutation	p.Thr238Met(p.T238M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359872
Start	33017611:33017611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1362T>G
AA Mutation	p.Ile454Met(p.I454M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359872
Start	34156120:34156120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754954730
CDS Mutation	c.413G>A
AA Mutation	p.Arg138Gln(p.R138Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359872
Start	33028245:33028245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.982C>T
AA Mutation	p.Pro328Ser(p.P328S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359872
Start	33021272:33021272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1235T>G
AA Mutation	p.Leu412Arg(p.L412R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359872
Start	33028259:33028259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968G>A
AA Mutation	p.Arg323His(p.R323H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359872
Start	33088960:33088960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.737T>A
AA Mutation	p.Val246Asp(p.V246D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359872
Start	33021242:33021242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1265C>T
AA Mutation	p.Ala422Val(p.A422V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359872
Start	34156336:34156336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201229528
CDS Mutation	c.197A>G
AA Mutation	p.Tyr66Cys(p.Y66C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359872
Start	34156367:34156367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359872
Start	34156403:34156403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359872
Start	33021241:33021241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759168920
CDS Mutation	c.1266G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359872
Start	33111987:33111987(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.636delG
AA Mutation	p.Thr213GlnfsTer32(p.T213Qfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359872
Start	33023999:33023999(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1058delA
AA Mutation	p.Lys353ArgfsTer14(p.K353Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359872
Start	33111986:33111987(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.636dupG
AA Mutation	p.Thr213AspfsTer15(p.T213Dfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000359872
Start	33088958:33088959(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.738_739insGGA
AA Mutation	p.Val246_Gln247insGly(p.V246_Q247insG)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ASIC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359872
Start	34156046:34156046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487G>T
AA Mutation	p.Asp163Tyr(p.D163Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359872
Start	33111986:33111987(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.636dupG
AA Mutation	p.Thr213AspfsTer15(p.T213Dfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000359872
Start	33017603:33017603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1368+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript