Colon Cancer: Gene >> BCLAF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136269542:136269542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2114G>T
AA Mutation	p.Ser705Ile(p.S705I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136276057:136276057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1468G>A
AA Mutation	p.Val490Ile(p.V490I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136278045:136278045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836A>T
AA Mutation	p.Asn279Ile(p.N279I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136278675:136278675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206G>T
AA Mutation	p.Arg69Leu(p.R69L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136278392:136278392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489A>C
AA Mutation	p.Glu163Asp(p.E163D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136261304:136261304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2718A>C
AA Mutation	p.Glu906Asp(p.E906D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136275690:136275690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1694T>C
AA Mutation	p.Leu565Ser(p.L565S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136267084:136267084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2489C>T
AA Mutation	p.Pro830Leu(p.P830L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136267067:136267067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2506G>A
AA Mutation	p.Asp836Asn(p.D836N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136267105:136267105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2468A>C
AA Mutation	p.Asn823Thr(p.N823T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136269603:136269603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2053A>C
AA Mutation	p.Lys685Gln(p.K685Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136278196:136278196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685C>T
AA Mutation	p.Pro229Ser(p.P229S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000531224
Start	136278557:136278557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756575094
CDS Mutation	c.324T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000531224
Start	136269454:136269454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2202A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000531224
Start	136278143:136278143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755222181
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000531224
Start	136268206:136268206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2353G>T
AA Mutation	p.Glu785Ter(p.E785*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000531224
Start	136276087:136276087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438G>T
AA Mutation	p.Glu480Ter(p.E480*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000531224
Start	136276159:136276159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1366G>T
AA Mutation	p.Glu456Ter(p.E456*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000531224
Start	136276432:136276432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093G>T
AA Mutation	p.Gly365Ter(p.G365*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BCLAF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136276052:136276052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1473G>T
AA Mutation	p.Lys491Asn(p.K491N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136267067:136267067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2506G>C
AA Mutation	p.Asp836His(p.D836H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000531224
Start	136276396:136276396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755260641
CDS Mutation	c.1129G>T
AA Mutation	p.Asp377Tyr(p.D377Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000531224
Start	136277984:136277984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000531224
Start	136275974:136275974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1551G>A
Mutation Classification	Silent
Feature Type	Transcript