Colon Cancer: Gene >> CARD10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251973
Start	37502618:37502618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1771C>G
AA Mutation	p.Leu591Val(p.L591V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000251973
Start	37508679:37508679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913G>A
AA Mutation	p.Ala305Thr(p.A305T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000251973
Start	37507882:37507882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762915999
CDS Mutation	c.1138C>T
AA Mutation	p.Arg380Cys(p.R380C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000251973
Start	37516145:37516145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201107638
CDS Mutation	c.527G>A
AA Mutation	p.Arg176Gln(p.R176Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000251973
Start	37516232:37516232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550531365
CDS Mutation	c.440G>A
AA Mutation	p.Arg147His(p.R147H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000251973
Start	37492743:37492743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755453339
CDS Mutation	c.2536C>T
AA Mutation	p.Arg846Trp(p.R846W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000251973
Start	37504660:37504660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770715620
CDS Mutation	c.1493T>C
AA Mutation	p.Met498Thr(p.M498T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000251973
Start	37491163:37491163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3095C>A
AA Mutation	p.Ala1032Asp(p.A1032D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251973
Start	37508566:37508566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1026G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251973
Start	37507853:37507853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1167G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251973
Start	37507913:37507913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373220389
CDS Mutation	c.1107G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251973
Start	37504242:37504242(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs747733671
CDS Mutation	c.1578delC
AA Mutation	p.Ser527ValfsTer31(p.S527Vfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251973
Start	37492501:37492501(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2685delC
AA Mutation	p.Lys896ArgfsTer9(p.K896Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000251973
Start	37506353:37506353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762039457
CDS Mutation	c.1222C>T
AA Mutation	p.Gln408Ter(p.Q408*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000251973
Start	37495866:37495866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144108378
CDS Mutation	c.2197C>T
AA Mutation	p.Arg733Ter(p.R733*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CARD10

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251973
Start	37504242:37504242(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs747733671
CDS Mutation	c.1578delC
AA Mutation	p.Ser527ValfsTer31(p.S527Vfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript