Colon Cancer: Gene >> RAD54B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336148
Start	94380306:94380306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2086A>C
AA Mutation	p.Ile696Leu(p.I696L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336148
Start	94467482:94467482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58T>A
AA Mutation	p.Phe20Ile(p.F20I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336148
Start	94391803:94391803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1615C>A
AA Mutation	p.Leu539Ile(p.L539I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336148
Start	94411279:94411279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.341A>G
AA Mutation	p.Glu114Gly(p.E114G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336148
Start	94391840:94391840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1578T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336148
Start	94391795:94391795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1623T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336148
Start	94458392:94458392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336148
Start	94380250:94380250(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2142delT
AA Mutation	p.Phe714LeufsTer5(p.F714Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000336148
Start	94399498:94399498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1294G>T
AA Mutation	p.Glu432Ter(p.E432*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000336148
Start	94411298:94411298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322G>T
AA Mutation	p.Glu108Ter(p.E108*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RAD54B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336148
Start	94391724:94391724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1694C>A
AA Mutation	p.Ser565Tyr(p.S565Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336148
Start	94391811:94391811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1607A>C
AA Mutation	p.Asn536Thr(p.N536T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000336148
Start	94400291:94400291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1117G>T
AA Mutation	p.Glu373Ter(p.E373*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000336148
Start	94400464:94400464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript