Colon Cancer: Gene >> RAD54L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371975
Start	46278248:46278248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2210A>G
AA Mutation	p.Gln737Arg(p.Q737R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371975
Start	46258699:46258699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745591449
CDS Mutation	c.224G>A
AA Mutation	p.Arg75Gln(p.R75Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371975
Start	46248563:46248563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.55T>C
AA Mutation	p.Ser19Pro(p.S19P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371975
Start	46267522:46267522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142375065
CDS Mutation	c.955C>T
AA Mutation	p.Arg319Trp(p.R319W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371975
Start	46260806:46260806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.557G>A
AA Mutation	p.Gly186Asp(p.G186D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371975
Start	46267515:46267515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371975
Start	46274574:46274574(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1730delG
AA Mutation	p.Gly577AlafsTer65(p.G577Afs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371975
Start	46272720:46272721(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1296dupA
AA Mutation	p.Pro433ThrfsTer7(p.P433Tfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RAD54L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371975
Start	46250096:46250096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187C>G
AA Mutation	p.Pro63Ala(p.P63A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371975
Start	46267473:46267473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759901390
CDS Mutation	c.906G>T
AA Mutation	p.Lys302Asn(p.K302N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371975
Start	46273697:46273697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1560G>A
Mutation Classification	Silent
Feature Type	Transcript