Colon Cancer: Gene >> GIMAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307194
Start	150720421:150720421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.417C>A
AA Mutation	p.Phe139Leu(p.F139L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307194
Start	150720902:150720902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752300708
CDS Mutation	c.898G>A
AA Mutation	p.Val300Ile(p.V300I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307194
Start	150720128:150720128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750341190
CDS Mutation	c.124G>A
AA Mutation	p.Ala42Thr(p.A42T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307194
Start	150720621:150720621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780854861
CDS Mutation	c.617G>A
AA Mutation	p.Gly206Glu(p.G206E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307194
Start	150720380:150720380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374968861
CDS Mutation	c.376G>A
AA Mutation	p.Ala126Thr(p.A126T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307194
Start	150720375:150720375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371T>C
AA Mutation	p.Phe124Ser(p.F124S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307194
Start	150720527:150720527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523C>T
AA Mutation	p.Arg175Cys(p.R175C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307194
Start	150720588:150720588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584G>A
AA Mutation	p.Arg195Gln(p.R195Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000307194
Start	150720318:150720318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314A>G
AA Mutation	p.Tyr105Cys(p.Y105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000307194
Start	150720900:150720900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896C>T
AA Mutation	p.Ala299Val(p.A299V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000307194
Start	150720587:150720587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Trp(p.R195W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307194
Start	150720343:150720343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370175882
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307194
Start	150720454:150720454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307194
Start	150720529:150720529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307194
Start	150720688:150720688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GIMAP1

No Mutation Annotation!