Colon Cancer: Gene >> SIAH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312960
Start	150742150:150742150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.966T>G
AA Mutation	p.Cys322Trp(p.C322W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312960
Start	150742233:150742233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748812007
CDS Mutation	c.883G>A
AA Mutation	p.Asp295Asn(p.D295N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312960
Start	150762755:150762755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95C>T
AA Mutation	p.Pro32Leu(p.P32L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312960
Start	150742365:150742365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137855704
CDS Mutation	c.751C>T
AA Mutation	p.Leu251Phe(p.L251F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312960
Start	150742240:150742240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876G>A
AA Mutation	p.Met292Ile(p.M292I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312960
Start	150742505:150742505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611T>C
AA Mutation	p.Val204Ala(p.V204A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312960
Start	150742372:150742372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751929587
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312960
Start	150742399:150742399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756788902
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312960
Start	150742591:150742591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SIAH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312960
Start	150742280:150742280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758857423
CDS Mutation	c.836C>T
AA Mutation	p.Thr279Met(p.T279M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312960
Start	150742528:150742528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.588C>A
Mutation Classification	Silent
Feature Type	Transcript