Colon Cancer: Gene >> HHAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261458
Start	210623583:210623583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1303T>C
AA Mutation	p.Ser435Pro(p.S435P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261458
Start	210623565:210623565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376491664
CDS Mutation	c.1285G>A
AA Mutation	p.Ala429Thr(p.A429T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261458
Start	210404558:210404558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563G>A
AA Mutation	p.Cys188Tyr(p.C188Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261458
Start	210464606:210464606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143700139
CDS Mutation	c.958G>A
AA Mutation	p.Ala320Thr(p.A320T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261458
Start	210418244:210418244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770748303
CDS Mutation	c.775G>A
AA Mutation	p.Glu259Lys(p.E259K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261458
Start	210623669:210623669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759828685
CDS Mutation	c.1389A>C
AA Mutation	p.Gln463His(p.Q463H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261458
Start	210623527:210623527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1247C>T
AA Mutation	p.Ala416Val(p.A416V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261458
Start	210464650:210464650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1002G>A
AA Mutation	p.Met334Ile(p.M334I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261458
Start	210623660:210623660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1380C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261458
Start	210588024:210588024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567965731
CDS Mutation	c.1170G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261458
Start	210404511:210404511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111463628
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261458
Start	210404619:210404619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745542930
CDS Mutation	c.624C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HHAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261458
Start	210349057:210349057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82G>T
AA Mutation	p.Val28Phe(p.V28F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261458
Start	210404505:210404505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261458
Start	210349059:210349059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.84C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000261458
Start	210623556:210623556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276C>T
AA Mutation	p.Arg426Ter(p.R426*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript