Colon Cancer: Gene >> HOXD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306324
Start	176152719:176152719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.545G>A
AA Mutation	p.Arg182His(p.R182H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306324
Start	176151754:176151754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121G>A
AA Mutation	p.Ala41Thr(p.A41T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306324
Start	176151712:176151712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79G>A
AA Mutation	p.Gly27Ser(p.G27S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306324
Start	176151751:176151751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.118G>A
AA Mutation	p.Gly40Ser(p.G40S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306324
Start	176151754:176151754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.121G>T
AA Mutation	p.Ala41Ser(p.A41S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306324
Start	176152761:176152761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754784160
CDS Mutation	c.587G>A
AA Mutation	p.Arg196His(p.R196H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306324
Start	176152824:176152824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650A>G
AA Mutation	p.Asn217Ser(p.N217S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306324
Start	176151647:176151647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14C>T
AA Mutation	p.Ser5Leu(p.S5L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306324
Start	176151762:176151762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306324
Start	176152751:176152751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.577C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306324
Start	176152927:176152927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367930048
CDS Mutation	c.753C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HOXD4

No Mutation Annotation!