Colon Cancer: Gene >> FGF10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264664
Start	44388599:44388599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199806461
CDS Mutation	c.84C>A
AA Mutation	p.Phe28Leu(p.F28L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264664
Start	44310473:44310473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383G>A
AA Mutation	p.Ser128Asn(p.S128N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264664
Start	44305010:44305010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.612G>T
AA Mutation	p.Met204Ile(p.M204I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264664
Start	44388480:44388480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203G>A
AA Mutation	p.Arg68Gln(p.R68Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264664
Start	44388385:44388385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298G>A
AA Mutation	p.Gly100Arg(p.G100R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264664
Start	44388576:44388576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107C>G
AA Mutation	p.Thr36Ser(p.T36S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264664
Start	44388522:44388522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161C>T
AA Mutation	p.Ser54Phe(p.S54F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264664
Start	44388444:44388444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239G>T
AA Mutation	p.Arg80Ile(p.R80I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264664
Start	44310502:44310502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201385181
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264664
Start	44388494:44388494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768676783
CDS Mutation	c.189G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000264664
Start	44310519:44310520(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.336_337insTGG
AA Mutation	p.Glu112_Ile113insTrp(p.E112_I113insW)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FGF10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264664
Start	44388415:44388415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268C>A
AA Mutation	p.Leu90Ile(p.L90I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript