Transcript #00019236 (NM_000358.2, TGFBI gene)

Transcript name transforming growth factor, beta-induced, 68kDa
Gene name TGFBI (transforming growth factor, beta-induced, 68kDa)
Chromosome 5
Transcript - NCBI ID NM_000358.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000349.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

187 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.135-43G>T r.(=) p.(=)
?/? c.135-41C>T r.(=) p.(=)
?/? c.135-4T>C r.spl? p.?
?/? c.141C>T r.(=) p.(=)
?/? c.216A>G r.(=) p.(=)
?/? c.224G>A r.(?) p.(Gly75Asp)
?/? c.233+3G>A r.spl? p.?
?/? c.233+26_233+27del r.(=) p.(=)
?/? c.233+41C>T r.(=) p.(=)
?/? c.233+42G>A r.(=) p.(=)
?/? c.233+47C>T r.(=) p.(=)
?/? c.233+52G>C r.(=) p.(=)
?/? c.234-53T>A r.(=) p.(=)
?/? c.240C>T r.(=) p.(=)
?/? c.246C>T r.(=) p.(=)
?/? c.298+1G>A r.spl? p.?
?/? c.298+15C>T r.(=) p.(=)
?/? c.298+44G>A r.(=) p.(=)
?/? c.298+49G>A r.(=) p.(=)
?/? c.299-46C>T r.(=) p.(=)
?/? c.299-34A>G r.(=) p.(=)
?/? c.322G>A r.(?) p.(Glu108Lys)
?/? c.327C>T r.(=) p.(=)
?/? c.346A>G r.(?) p.(Thr116Ala)
?/? c.362A>G r.(?) p.(Tyr121Cys)
?/? c.374C>G r.(?) p.(Thr125Arg)
?/? c.404C>T r.(?) p.(Pro135Leu)
?/? c.419T>C r.(?) p.(Ile140Thr)
?/? c.431G>A r.(?) p.(Ser144Asn)
?/? c.447C>G r.(=) p.(=)
?/? c.459+15G>A r.(=) p.(=)
?/? c.459+27G>C r.(=) p.(=)
?/? c.459+30T>A r.(=) p.(=)
?/? c.459+31C>A r.(=) p.(=)
?/? c.459+34A>G r.(=) p.(=)
?/? c.460-17C>T r.(=) p.(=)
?/? c.460-16C>T r.(=) p.(=)
?/? c.486T>C r.(=) p.(=)
?/? c.494T>C r.(?) p.(Ile165Thr)
?/? c.496G>A r.(?) p.(Glu166Lys)
?/? c.514C>T r.(?) p.(Arg172Cys)
?/? c.523A>G r.(?) p.(Met175Val)
?/? c.536G>A r.(?) p.(Arg179Gln)
?/? c.561C>T r.(=) p.(=)
?/? c.580A>G r.(?) p.(Met194Val)
?/? c.585C>T r.(=) p.(=)
?/? c.594C>T r.(=) p.(=)
?/? c.598A>T r.(?) p.(Ile200Phe)
?/? c.624+23G>T r.(=) p.(=)
?/? c.625-49C>T r.(=) p.(=)
?/? c.625-39G>C r.(=) p.(=)
?/? c.625-17G>C r.(=) p.(=)
?/? c.625-3C>A r.spl? p.?
?/? c.630A>G r.(=) p.(=)
?/? c.647G>T r.(?) p.(Arg216Leu)
?/? c.651G>C r.(=) p.(=)
?/? c.678C>T r.(=) p.(=)
?/? c.690C>T r.(=) p.(=)
?/? c.696C>T r.(=) p.(=)
?/? c.739A>C r.(?) p.(Ile247Leu)
?/? c.740T>C r.(?) p.(Ile247Thr)
?/? c.770G>A r.(?) p.(Arg257Gln)
?/? c.772-26C>G r.(=) p.(=)
?/? c.805C>T r.(?) p.(Leu269Phe)
?/? c.816C>T r.(=) p.(=)
?/? c.817G>A r.(?) p.(Gly273Ser)
?/? c.829C>G r.(?) p.(Leu277Val)
?/? c.842C>A r.(?) p.(Thr281Asn)
?/? c.852C>A r.(=) p.(=)
?/? c.856G>A r.(?) p.(Glu286Lys)
?/? c.895G>A r.(?) p.(Asp299Asn)
?/? c.913+3G>T r.spl? p.?
?/? c.913+38G>A r.(=) p.(=)
?/? c.913+47T>C r.(=) p.(=)
?/? c.914-44C>T r.(=) p.(=)
?/? c.914-29G>A r.(=) p.(=)
?/? c.952G>A r.(?) p.(Ala318Thr)
?/? c.963C>T r.(=) p.(=)
?/? c.968C>T r.(?) p.(Ala323Val)
?/? c.981A>G r.(=) p.(=)
?/? c.1000A>G r.(?) p.(Thr334Ala)
?/? c.1027A>G r.(?) p.(Met343Val)
?/? c.1042G>T r.(?) p.(Gly348Trp)
?/? c.1050G>A r.(=) p.(=)
?/? c.1061A>G r.(?) p.(Asn354Ser)
?/? c.1083C>T r.(=) p.(=)
?/? c.1126+12C>T r.(=) p.(=)
?/? c.1126+15C>T r.(=) p.(=)
?/? c.1126+20G>T r.(=) p.(=)
?/? c.1126+43A>G r.(=) p.(=)
?/? c.1127-50A>C r.(=) p.(=)
?/? c.1127-39C>T r.(=) p.(=)
?/? c.1127-11C>T r.(=) p.(=)
?/? c.1167C>T r.(=) p.(=)
?/? c.1202G>T r.(?) p.(Gly401Val)
?/? c.1264+23G>A r.(=) p.(=)
?/? c.1265-39G>A r.(=) p.(=)
?/? c.1265-11C>T r.(=) p.(=)
?/? c.1306C>T r.(?) p.(Arg436Trp)
?/? c.1329G>T r.(?) p.(Gln443His)
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