Transcript #00025443 (NM_005560.4, LAMA5 gene)

Transcript name laminin, alpha 5
Gene name LAMA5 (laminin, alpha 5)
Chromosome 20
Transcript - NCBI ID NM_005560.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_005551.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2019-07-18 10:42:49 +02:00 (CEST)
Date last edited N/A


Variants

236 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.? r.(?) p.(Gly3067Alafs*40)
?/. - c.? r.(?) p.(Pro1082Leu)
?/. - c.? r.(?) p.(Leu1930Pro)
-?/. - c.125G>A r.(?) p.(Gly42Asp)
?/. - c.371C>T r.(?) p.(Thr124Met)
?/. - c.403C>T r.(?) p.(Arg135Cys)
?/. - c.418A>C r.(?) p.(Asn140His)
-?/. - c.450+18C>T r.(=) p.(=)
?/. - c.535G>A r.(?) p.(Gly179Ser)
?/. - c.617G>A r.(?) p.(Arg206His)
?/. - c.617G>A r.(?) p.(Arg206His)
-/. - c.638C>T r.(?) p.(Ala213Val)
?/. - c.740C>T r.(?) p.(Ser247Leu)
?/. - c.743C>T r.(?) p.(Pro248Leu)
?/. - c.812G>A r.(?) p.(Gly271Asp)
-/. - c.888C>T r.(?) p.(=)
-?/. - c.918G>A r.(?) p.(=)
-?/. - c.950C>T r.(?) p.(Pro317Leu)
?/. - c.1003C>T r.(?) p.(Arg335Cys)
?/. - c.1132C>T r.(?) p.(Arg378Cys)
-?/. - c.1134C>T r.(?) p.(=)
-/. - c.1134C>T r.(?) p.(=)
-?/. - c.1299C>T r.(?) p.(=)
-?/. - c.1443C>T r.(?) p.(=)
-/. - c.1478-4C>G r.spl? p.?
?/. - c.1754A>G r.(?) p.(Gln585Arg)
-?/. - c.1891+8G>A r.(=) p.(=)
-?/. - c.1892-15A>G r.(=) p.(=)
-?/. - c.1892-8C>T r.(=) p.(=)
-?/. - c.1892-8C>T r.(=) p.(=)
-/. - c.2049C>G r.(?) p.(Gly683=)
-?/. - c.2126C>T r.(?) p.(Thr709Ile)
-?/. - c.2126C>T r.(?) p.(Thr709Ile)
-?/. - c.2285T>G r.(?) p.(Phe762Cys)
-?/. - c.2285T>G r.(?) p.(Phe762Cys)
-?/. - c.2321C>T r.(?) p.(Thr774Ile)
-?/. - c.2321C>T r.(?) p.(Thr774Ile)
-?/. - c.2323C>T r.(?) p.(Arg775Cys)
?/. - c.2375C>T r.(?) p.(Pro792Leu)
-?/. - c.2382C>T r.(?) p.(Thr794=)
-?/. - c.2382C>T r.(?) p.(Thr794=)
?/. - c.2383G>A r.(?) p.(Gly795Ser)
?/. - c.2389_2418dup r.(?) p.(Cys797_Gln806dup)
-?/. - c.2412C>T r.(?) p.(=)
?/. - c.2413G>A r.(?) p.(Gly805Ser)
-/. - c.2435A>C r.(?) p.(Lys812Thr)
-?/. - c.2588C>T r.(?) p.(Ala863Val)
?/. - c.2719G>A r.(?) p.(Ala907Thr)
?/. - c.2735T>G r.(?) p.(Val912Gly)
-?/. - c.2740-17G>C r.(=) p.(=)
?/. - c.2829C>T r.(?) p.(=)
-?/. - c.2919G>A r.(?) p.(=)
-?/. - c.3027C>T r.(?) p.(Tyr1009=)
-?/. - c.3062C>T r.(?) p.(Ala1021Val)
-?/. - c.3066C>T r.(?) p.(Leu1022=)
-?/. - c.3129-3C>A r.spl? p.?
?/. - c.3231G>A r.(?) p.(Thr1077=)
-?/. - c.3252C>T r.(?) p.(=)
-?/. - c.3265A>T r.(?) p.(Thr1089Ser)
-/. - c.3283-8C>G r.(=) p.(=)
-?/. - c.3295C>T r.(?) p.(Leu1099Phe)
?/. - c.3376G>A r.(?) p.(Val1126Met)
-?/. - c.3444-5del r.spl? p.?
-?/. - c.3444-5del r.spl? p.?
-?/. - c.3606C>G r.(?) p.(Pro1202=)
-?/. - c.3633C>T r.(?) p.(Gly1211=)
?/. - c.3815A>G r.(?) p.(Asp1272Gly)
-?/. - c.3885G>A r.(?) p.(Thr1295=)
-?/. - c.3963C>T r.(?) p.(Ala1321=)
?/. - c.3964G>A r.(?) p.(Gly1322Ser)
-?/. - c.3979+16G>T r.(=) p.(=)
?/. - c.4072G>A r.(?) p.(Glu1358Lys)
?/. - c.4465C>T r.(?) p.(Arg1489Cys)
-?/. - c.4595G>A r.(?) p.(Gly1532Glu)
-?/. - c.4599C>T r.(?) p.(Pro1533=)
?/. - c.4675C>T r.(?) p.(Arg1559Cys)
?/. - c.4697C>T r.(?) p.(Pro1566Leu)
-?/. - c.4713C>T r.(?) p.(Tyr1571=)
-?/. - c.4724G>A r.(?) p.(Arg1575His)
-?/. - c.4754C>T r.(?) p.(Ala1585Val)
-?/. - c.4757C>T r.(?) p.(Pro1586Leu)
?/. - c.4879C>T r.(?) p.(Arg1627Cys)
-?/. - c.4913G>A r.(?) p.(Arg1638Gln)
-?/. - c.4939-15C>T r.(=) p.(=)
-?/. - c.4999C>T r.(?) p.(Arg1667Trp)
-?/. - c.5035C>T r.(?) p.(Arg1679Trp)
-?/. - c.5070C>T r.(?) p.(Pro1690=)
?/. - c.5110C>T r.(?) p.(Arg1704Trp)
-/. - c.5124C>T r.(?) p.(=)
-?/. - c.5203G>A r.(?) p.(Val1735Met)
-?/. - c.5269G>A r.(?) p.(Val1757Ile)
?/. - c.5309G>A r.(?) p.(Arg1770Gln)
-?/. - c.5513G>A r.(?) p.(Arg1838Gln)
-?/. - c.5530-13C>T r.(=) p.(=)
-?/. - c.5627G>T r.(?) p.(Gly1876Val)
-?/. - c.5634C>T r.(?) p.(Gly1878=)
+/. - c.5681_5736del r.(?) p.(Arg1894Leufs*64)
-?/. - c.5708G>A r.(?) p.(Arg1903Lys)
-/. - c.5709G>A r.(?) p.(Arg1903=)
-?/. - c.5713G>A r.(?) p.(Asp1905Asn)
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