Colon Cancer: Gene >> TTLL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298832
Start	75776811:75776811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2348T>G
AA Mutation	p.Val783Gly(p.V783G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298832
Start	75681587:75681587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751047559
CDS Mutation	c.224G>A
AA Mutation	p.Arg75His(p.R75H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298832
Start	75745526:75745526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778757743
CDS Mutation	c.1432C>T
AA Mutation	p.Arg478Trp(p.R478W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298832
Start	75882763:75882763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3601G>A
AA Mutation	p.Ala1201Thr(p.A1201T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000298832
Start	75681575:75681575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775184984
CDS Mutation	c.212G>A
AA Mutation	p.Arg71Gln(p.R71Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000298832
Start	75782487:75782487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2516A>G
AA Mutation	p.Asp839Gly(p.D839G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000298832
Start	75863716:75863716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3376G>T
AA Mutation	p.Val1126Leu(p.V1126L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000298832
Start	75779593:75779593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2406G>T
AA Mutation	p.Glu802Asp(p.E802D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000298832
Start	75764620:75764620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1556C>T
AA Mutation	p.Thr519Ile(p.T519I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000298832
Start	75752903:75752903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1498G>A
AA Mutation	p.Glu500Lys(p.E500K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000298832
Start	75775509:75775509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746631669
CDS Mutation	c.2162G>A
AA Mutation	p.Arg721Gln(p.R721Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298832
Start	75719762:75719762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.870T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298832
Start	75882717:75882717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3555C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000298832
Start	75783434:75783434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777359273
CDS Mutation	c.2890C>T
AA Mutation	p.Arg964Ter(p.R964*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000298832
Start	75782574:75782574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2602+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000298832
Start	75707089:75707089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TTLL5

No Mutation Annotation!