Colon Cancer: Gene >> TAF1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263663
Start	9875958:9875958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.647C>T
AA Mutation	p.Ala216Val(p.A216V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263663
Start	9868408:9868408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.532G>A
AA Mutation	p.Val178Ile(p.V178I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263663
Start	9919806:9919806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1551G>T
AA Mutation	p.Gln517His(p.Q517H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263663
Start	9904885:9904885(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.834delC
AA Mutation	p.Tyr278Ter(p.Y278*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000263663
Start	9904886:9904886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.835A>T
AA Mutation	p.Lys279Ter(p.K279*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000263663
Start	9910738:9910738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958G>T
AA Mutation	p.Glu320Ter(p.E320*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000263663
Start	9849442:9849444(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.195_197delAAA
AA Mutation	p.Lys65del(p.K65del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000263663
Start	9919778:9919779(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1523_1524insATTGTTTCT
AA Mutation	p.Lys508_Asn509insLeuPheLeu(p.K508_N509insLFL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TAF1B

No Mutation Annotation!