Colon Cancer: Gene >> ABCB7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373394
Start	75053469:75053469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2160G>T
AA Mutation	p.Trp720Cys(p.W720C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373394
Start	75060285:75060285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1981A>C
AA Mutation	p.Ile661Leu(p.I661L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373394
Start	75099019:75099019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376T>C
AA Mutation	p.Ser126Pro(p.S126P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373394
Start	75073765:75073765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.956G>T
AA Mutation	p.Arg319Ile(p.R319I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373394
Start	75062387:75062387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1876G>A
AA Mutation	p.Asp626Asn(p.D626N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373394
Start	75099055:75099055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340G>T
AA Mutation	p.Asp114Tyr(p.D114Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373394
Start	75069089:75069089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1577A>G
AA Mutation	p.Lys526Arg(p.K526R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373394
Start	75070477:75070477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1253T>G
AA Mutation	p.Phe418Cys(p.F418C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373394
Start	75073945:75073945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769487666
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373394
Start	75069389:75069389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1431G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373394
Start	75075596:75075596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199727121
CDS Mutation	c.621C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373394
Start	75075563:75075563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.654C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000373394
Start	75065235:75065236(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1665_1666insTGA
AA Mutation	p.Ala555_Val556insTer(p.A555_V556ins*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ABCB7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373394
Start	75062341:75062341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1922C>T
AA Mutation	p.Ser641Leu(p.S641L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373394
Start	75069082:75069082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1584C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373394
Start	75114790:75114790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.210A>G
Mutation Classification	Silent
Feature Type	Transcript