Colon Cancer: Gene >> SDHA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	233572:233572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200526913
CDS Mutation	c.991G>A
AA Mutation	p.Ala331Thr(p.A331T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	251013:251013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1573G>A
AA Mutation	p.Val525Met(p.V525M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	251004:251004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1564C>A
AA Mutation	p.His522Asn(p.H522N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	225938:225938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587782076
CDS Mutation	c.512G>A
AA Mutation	p.Arg171His(p.R171H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	251452:251452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1778C>T
AA Mutation	p.Ala593Val(p.A593V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	251031:251031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371056571
CDS Mutation	c.1591G>A
AA Mutation	p.Val531Met(p.V531M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	230884:230884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.779G>T
AA Mutation	p.Gly260Val(p.G260V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	235214:235214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749309213
CDS Mutation	c.1135C>T
AA Mutation	p.Arg379Cys(p.R379C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	224366:224366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157G>A
AA Mutation	p.Ala53Thr(p.A53T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	228269:228269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774160524
CDS Mutation	c.706G>A
AA Mutation	p.Ala236Thr(p.A236T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	233559:233559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978T>A
AA Mutation	p.Phe326Leu(p.F326L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	251440:251440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763766162
CDS Mutation	c.1766G>A
AA Mutation	p.Arg589Gln(p.R589Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	228219:228219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756877901
CDS Mutation	c.656A>G
AA Mutation	p.Tyr219Cys(p.Y219C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264932
Start	235255:235255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1041950
CDS Mutation	c.1176C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264932
Start	235312:235312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376530094
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000264932
Start	224432:224432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781764920
CDS Mutation	c.223C>T
AA Mutation	p.Arg75Ter(p.R75*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000264932
Start	251414:251414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1740C>G
AA Mutation	p.Tyr580Ter(p.Y580*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SDHA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	225473:225473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367T>A
AA Mutation	p.Phe123Ile(p.F123I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	228306:228306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743G>C
AA Mutation	p.Arg248Thr(p.R248T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264932
Start	228257:228257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694C>T
AA Mutation	p.Arg232Cys(p.R232C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript