Colon Cancer: Gene >> ZACN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334586
Start	76082517:76082517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751792417
CDS Mutation	c.1103G>A
AA Mutation	p.Arg368His(p.R368H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334586
Start	76079473:76079473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.132G>T
AA Mutation	p.Lys44Asn(p.K44N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334586
Start	76081344:76081344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611T>C
AA Mutation	p.Val204Ala(p.V204A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334586
Start	76079543:76079543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202G>A
AA Mutation	p.Val68Ile(p.V68I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334586
Start	76082640:76082640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746472319
CDS Mutation	c.1226G>A
AA Mutation	p.Arg409Gln(p.R409Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334586
Start	76081897:76081897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.896T>C
AA Mutation	p.Ile299Thr(p.I299T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334586
Start	76081565:76081565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762932459
CDS Mutation	c.690G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000334586
Start	76079711:76079711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140302218
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Ter(p.R78*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000334586
Start	76079995:76079995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529296856
CDS Mutation	c.374+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000334586
Start	76079734:76079742(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.259_267delCTTAGGCTG
AA Mutation	p.Leu87_Leu89del(p.L87_L89del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZACN

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334586
Start	76081399:76081399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201632789
CDS Mutation	c.666G>A
Mutation Classification	Silent
Feature Type	Transcript