Colon Cancer: Gene >> TMEM132A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60936567:60936567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142666359
CDS Mutation	c.2732G>A
AA Mutation	p.Arg911Gln(p.R911Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60933623:60933623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151003082
CDS Mutation	c.1438C>T
AA Mutation	p.Arg480Cys(p.R480C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60928890:60928890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140281492
CDS Mutation	c.796C>T
AA Mutation	p.Arg266Trp(p.R266W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60927266:60927266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749594128
CDS Mutation	c.163G>A
AA Mutation	p.Ala55Thr(p.A55T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60927852:60927852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144441365
CDS Mutation	c.527G>A
AA Mutation	p.Arg176His(p.R176H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60935358:60935358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566743806
CDS Mutation	c.1943C>T
AA Mutation	p.Ser648Leu(p.S648L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60928891:60928891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.797G>T
AA Mutation	p.Arg266Leu(p.R266L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60932041:60932041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566097839
CDS Mutation	c.1270C>T
AA Mutation	p.Arg424Cys(p.R424C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60928891:60928891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777345475
CDS Mutation	c.797G>A
AA Mutation	p.Arg266Gln(p.R266Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60935423:60935423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2008G>A
AA Mutation	p.Ala670Thr(p.A670T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60936465:60936465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140765233
CDS Mutation	c.2630G>A
AA Mutation	p.Arg877His(p.R877H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60930584:60930584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.941A>G
AA Mutation	p.Asp314Gly(p.D314G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453848
Start	60933562:60933562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765219109
CDS Mutation	c.1377C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453848
Start	60930627:60930627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376774818
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453848
Start	60935950:60935950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2115C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453848
Start	60928793:60928793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000453848
Start	60932062:60932062(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1297delG
AA Mutation	p.Ala433ProfsTer5(p.A433Pfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000453848
Start	60936704:60936704(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2874delG
AA Mutation	p.Arg959GlyfsTer5(p.R959Gfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000453848
Start	60931747:60931747(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1079delG
AA Mutation	p.Gly360AlafsTer2(p.G360Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000453848
Start	60933597:60933597(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1417delG
AA Mutation	p.Val473CysfsTer16(p.V473Cfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000453848
Start	60933660:60933660(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1480delC
AA Mutation	p.Leu494CysfsTer82(p.L494Cfs*82)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000453848
Start	60928822:60928823(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.734dupC
AA Mutation	p.Gln246AlafsTer17(p.Q246Afs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM132A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000453848
Start	60936872:60936872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749168270
CDS Mutation	c.3037C>T
AA Mutation	p.Arg1013Cys(p.R1013C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript