Colon Cancer: Gene >> HOXD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249440
Start	176171585:176171585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610G>A
AA Mutation	p.Ala204Thr(p.A204T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249440
Start	176171721:176171721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746A>G
AA Mutation	p.Tyr249Cys(p.Y249C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249440
Start	176171586:176171586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611C>T
AA Mutation	p.Ala204Val(p.A204V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000249440
Start	176171719:176171719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.744G>T
AA Mutation	p.Lys248Asn(p.K248N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000249440
Start	176171732:176171732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.757C>A
AA Mutation	p.Gln253Lys(p.Q253K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249440
Start	176172151:176172151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760834566
CDS Mutation	c.1176C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249440
Start	176171833:176171833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249440
Start	176169237:176169237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201012462
CDS Mutation	c.123C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249440
Start	176172046:176172046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201412033
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249440
Start	176172013:176172013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249440
Start	176172115:176172115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1140G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000249440
Start	176169415:176169415(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.305delG
AA Mutation	p.Gly102ValfsTer9(p.G102Vfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000249440
Start	176169655:176169655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.541G>T
AA Mutation	p.Gly181Ter(p.G181*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HOXD3

No Mutation Annotation!