Transcript #00025926 (NM_001394062.1, MACF1 gene)

Transcript name transcript variant 2 (removed from reference sequence)
Gene name MACF1 (microtubule-actin crosslinking factor 1)
Chromosome 1
Transcript - NCBI ID NM_001394062.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001380991.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks MANE select
Date created 2024-05-22 09:07:24 +02:00 (CEST)
Date last edited N/A


Variants

90 entries on 1 page. Showing entries 1 - 90.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.172-6400A>T r.(=) p.(=)
?/. - c.467T>G r.(?) p.(Ile156Ser)
?/. - c.950G>T r.(?) p.(Arg317Leu)
?/. - c.2567G>A r.(?) p.(Arg856His)
-?/. - c.2594C>T r.(?) p.(Thr865Ile)
-?/. - c.3032T>C r.(?) p.(Leu1011Ser)
?/. - c.3265dup r.(?) p.(Gln1089Profs*23)
?/. - c.3422A>G r.(?) p.(Tyr1141Cys)
?/. - c.3471A>G r.(?) p.(Ile1157Met)
-?/. - c.3782G>A r.(?) p.(Arg1261His)
?/. - c.3821A>G r.(?) p.(Asp1274Gly)
?/. - c.4229A>T r.(?) p.(Glu1410Val)
?/. - c.4389+3G>C r.spl? p.?
?/. - c.4394T>G r.(?) p.(Leu1465Arg)
-?/. - c.4615-12_4615-2del r.spl? p.?
-?/. - c.10874T>C r.(?) p.(Val3625Ala)
-?/. - c.10966-6G>A r.(=) p.(=)
-?/. - c.10991G>A r.(?) p.(Arg3664His)
?/. - c.11027A>C r.(?) p.(Glu3676Ala)
-?/. - c.11080C>T r.(?) p.(Leu3694Phe)
?/. - c.11080C>T r.(?) p.(Leu3694Phe)
?/. - c.11080C>T r.(?) p.(Leu3694Phe)
-?/. - c.11135C>T r.(?) p.(Thr3712Ile)
?/. - c.11135C>T r.(?) p.(Thr3712Ile)
?/. - c.11135C>T r.(?) p.(Thr3712Ile)
?/. - c.11372T>G r.(?) p.(Met3791Arg)
?/. - c.12025T>C r.(?) p.(Trp4009Arg)
-?/. - c.12057G>C r.(?) p.(Lys4019Asn)
-?/. - c.12454-7A>C r.(=) p.(=)
?/. - c.12851G>A r.(?) p.(Gly4284Asp)
?/. - c.13421A>G r.(?) p.(Gln4474Arg)
?/. - c.13484C>T r.(?) p.(Thr4495Ile)
?/. - c.13549C>T r.(?) p.(Pro4517Ser)
-?/. - c.13807A>G r.(?) p.(Ile4603Val)
?/. - c.13887T>A r.(?) p.(His4629Gln)
?/. - c.13997A>G r.(?) p.(Glu4666Gly)
?/. - c.14214C>G r.(?) p.(His4738Gln)
?/. - c.14350C>T r.(?) p.(Arg4784Cys)
-?/. - c.14696A>G r.(?) p.(Lys4899Arg)
-?/. - c.14842A>G r.(?) p.(Met4948Val)
-/. - c.15005C>G r.(?) p.(Thr5002Arg)
?/. - c.15196G>A r.(?) p.(Val5066Ile)
-?/. - c.15398C>T r.(?) p.(Ser5133Phe)
-?/. - c.15478G>A r.(?) p.(Glu5160Lys)
-?/. - c.15548G>A r.(?) p.(Cys5183Tyr)
-?/. - c.15650A>C r.(?) p.(Lys5217Thr)
-?/. - c.15728C>T r.(?) p.(Ala5243Val)
-?/. - c.15769G>C r.(?) p.(Val5257Leu)
?/. - c.15776C>A r.(?) p.(Thr5259Asn)
-?/. - c.15787A>G r.(?) p.(Ile5263Val)
?/. - c.15817-10995G>C r.(=) p.(=)
?/. - c.15817-10745C>G r.(=) p.(=)
?/. - c.15817-10719G>T r.(=) p.(=)
-?/. - c.15817-10551C>T r.(=) p.(=)
?/. - c.15817-9572C>T r.(=) p.(=)
-?/. - c.15920A>G r.(?) p.(Gln5307Arg)
-?/. - c.16175G>A r.(?) p.(Arg5392Gln)
-?/. - c.16242T>G r.(?) p.(Asp5414Glu)
?/. - c.16468C>T r.(?) p.(Arg5490Trp)
?/. - c.16927A>G r.(?) p.(Ile5643Val)
+?/. - c.17014C>T r.(?) p.(Gln5672*)
-?/. - c.17131-9C>G r.(=) p.(=)
-?/. - c.17144A>C r.(?) p.(Glu5715Ala)
-?/. - c.17287A>G r.(?) p.(Ile5763Val)
-?/. - c.17515C>T r.(?) p.(Arg5839Cys)
?/. - c.18073G>C r.(?) p.(Val6025Leu)
-?/. - c.18104A>G r.(?) p.(Asn6035Ser)
-?/. - c.18274C>T r.(?) p.(Arg6092Trp)
?/. - c.18634G>T r.(?) p.(Ala6212Ser)
-?/. - c.19030G>A r.(?) p.(Glu6344Lys)
?/. - c.19070C>T r.(?) p.(Pro6357Leu)
-?/. - c.19230G>T r.(?) p.(Met6410Ile)
-?/. - c.19303-9dup r.(=) p.(=)
?/. - c.19670A>G r.(?) p.(Asn6557Ser)
-?/. - c.19823A>G r.(?) p.(Asn6608Ser)
?/. - c.20001G>T r.(?) p.(Trp6667Cys)
?/. - c.20007A>C r.(?) p.(Glu6669Asp)
-?/. - c.20179G>A r.(?) p.(Glu6727Lys)
-?/. - c.20616G>A r.(?) p.(Ala6872=)
+?/. - c.20719C>T r.(?) p.(Gln6907Ter)
-?/. - c.21032C>T r.(?) p.(Pro7011Leu)
-?/. - c.21075+3A>G r.spl? p.?
?/. - c.21580G>A r.(?) p.(Gly7194Arg)
?/. - c.21802C>T r.(?) p.(Arg7268Cys)
?/. - c.22022G>A r.(?) p.(Gly7341Glu)
?/. - c.22036C>T r.(?) p.(Arg7346Cys)
-?/. - c.22282-6T>G r.(=) p.(=)
-?/. - c.22340G>A r.(?) p.(Arg7447Gln)
?/. - c.22446_22457del r.(?) p.(Gly7488_Ala7491del)
?/. - c.22446_22457del r.(?) p.(Gly7488_Ala7491del)
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