Colon Cancer: Gene >> SYDE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342784
Start	15112420:15112420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1653G>T
AA Mutation	p.Gln551His(p.Q551H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342784
Start	15113649:15113649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1894G>A
AA Mutation	p.Glu632Lys(p.E632K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342784
Start	15109169:15109169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202G>A
AA Mutation	p.Ala68Thr(p.A68T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000342784
Start	15109056:15109056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.89G>A
AA Mutation	p.Gly30Asp(p.G30D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000342784
Start	15111380:15111380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140575092
CDS Mutation	c.1358G>A
AA Mutation	p.Arg453Gln(p.R453Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000342784
Start	15113670:15113670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1915G>A
AA Mutation	p.Gly639Ser(p.G639S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000342784
Start	15110676:15110676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753753794
CDS Mutation	c.1231G>A
AA Mutation	p.Gly411Ser(p.G411S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000342784
Start	15112376:15112376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1609C>T
AA Mutation	p.Arg537Cys(p.R537C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000342784
Start	15113886:15113886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2131C>A
AA Mutation	p.Leu711Met(p.L711M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000342784
Start	15110707:15110707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1262T>C
AA Mutation	p.Val421Ala(p.V421A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342784
Start	15109102:15109102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.135C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342784
Start	15109246:15109246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342784
Start	15110329:15110329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1056G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342784
Start	15112498:15112498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1731C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342784
Start	15113882:15113882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775739044
CDS Mutation	c.2127G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342784
Start	15113852:15113852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2097C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342784
Start	15113864:15113864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2109C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000342784
Start	15111652:15111652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438C>T
AA Mutation	p.Arg480Ter(p.R480*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SYDE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342784
Start	15109715:15109715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442G>A
AA Mutation	p.Ala148Thr(p.A148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342784
Start	15111421:15111421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552391083
CDS Mutation	c.1399G>A
AA Mutation	p.Asp467Asn(p.D467N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342784
Start	15113864:15113864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2109C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342784
Start	15110213:15110213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940C>A
Mutation Classification	Silent
Feature Type	Transcript