Transcript #00010944 (NM_002291.2, LAMB1 gene)

Transcript name laminin, beta 1
Gene name LAMB1 (laminin, beta 1)
Chromosome 7
Transcript - NCBI ID NM_002291.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_002282.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.298G>A r.(?) p.(Val100Ile)
?/. - c.463G>A r.(?) p.(Asp155Asn)
-?/. - c.468T>C r.(?) p.(Phe156=)
?/. - c.476C>G r.(?) p.(Thr159Ser)
?/. - c.506A>G r.(?) p.(Asp169Gly)
?/. - c.536C>A r.(?) p.(Thr179Asn)
-?/. - c.816C>T r.(?) p.(=)
?/. - c.949C>G r.(?) p.(His317Asp)
-?/. - c.1000+7C>T r.(=) p.(=)
+/. - c.1001-1G>C r.spl? p.?
?/. - c.1103A>G r.(?) p.(Asn368Ser)
-?/. - c.1135C>T r.(?) p.(Pro379Ser)
-/. - c.1135C>T r.(?) p.(Pro379Ser)
?/. - c.1447C>T r.(?) p.(Arg483Cys)
?/. - c.1563-54G>A r.(=) p.(=)
?/. - c.1571C>T r.(?) p.(Ala524Val)
-?/. - c.1590A>C r.(?) p.(Ser530=)
-?/. - c.1593C>T r.(?) p.(Cys531=)
?/. - c.1698+3G>C r.spl? p.?
-/. - c.1776T>G r.(?) p.(Pro592=)
-?/. - c.1944C>T r.(?) p.(Pro648=)
?/. - c.2109+2_2109+3insTT r.spl? p.?
?/. - c.2248C>A r.(?) p.(Pro750Thr)
-?/. - c.2250G>A r.(?) p.(Pro750=)
-?/. - c.2314+10G>T r.(=) p.(=)
?/. - c.2326G>A r.(?) p.(Asp776Asn)
?/. - c.2363A>G r.(?) p.(Asn788Ser)
+?/. - c.2363A>G r.(?) p.(Asn788Ser)
?/. - c.2411A>G r.(?) p.(Asn804Ser)
-?/. - c.2459-10G>A r.(=) p.(=)
?/. - c.2528T>C r.(?) p.(Phe843Ser)
?/. - c.2537T>C r.(?) p.(Val846Ala)
?/. - c.2545C>G r.(?) p.(Arg849Gly)
?/. - c.2557C>T r.(?) p.(Arg853Trp)
?/. - c.2576G>T r.(?) p.(Trp859Leu)
-?/. - c.2616C>T r.(?) p.(His872=)
-?/. - c.2619C>T r.(?) p.(Ala873=)
-?/. - c.2691-9C>T r.(=) p.(=)
?/. - c.2701G>T r.(?) p.(Gly901Cys)
?/. - c.2723T>C r.(?) p.(Ile908Thr)
?/. - c.2882G>A r.(?) p.(Gly961Glu)
-/. - c.2920C>G r.(?) p.(Gln974Glu)
?/. - c.2951C>G r.(?) p.(Thr984Arg)
-?/. - c.2988G>A r.(?) p.(Arg996=)
?/. - c.3025dup r.(?) p.(Cys1009Leufs*11)
?/. - c.3037C>T r.(?) p.(Arg1013Trp)
-/. - c.3065A>G r.(?) p.(Gln1022Arg)
?/. - c.3124G>A r.(?) p.(Gly1042Ser)
-?/. - c.3165G>C r.(?) p.(Leu1055Phe)
?/. - c.3194G>A r.(?) p.(Cys1065Tyr)
?/. - c.3199C>T r.(?) p.(Arg1067Cys)
?/. - c.3277G>A r.(?) p.(Gly1093Arg)
-?/. - c.3279G>T r.(?) p.(Gly1093=)
?/. - c.3388C>T r.(?) p.(Arg1130*)
?/. - c.3469G>T r.(?) p.(Val1157Phe)
?/. - c.3509C>T r.(?) p.(Ser1170Leu)
./. - c.3543G>C r.(?) p.(Gln1181His)
-?/. - c.3573C>T r.(?) p.(Ala1191=)
-?/. - c.3630T>C r.(?) p.(Ser1210=)
-?/. - c.3642G>T r.(?) p.(Gly1214=)
-?/. - c.3687G>A r.(?) p.(Glu1229=)
?/. - c.3695A>G r.(?) p.(Asp1232Gly)
+?/. - c.3803_3804dup r.(?) p.(Val1269LysfsTer2)
?/. - c.3992C>G r.(?) p.(Ala1331Gly)
?/. - c.4034C>G r.(?) p.(Thr1345Ser)
?/. - c.4036G>C r.(?) p.(Val1346Leu)
-?/. - c.4114G>A r.(?) p.(Glu1372Lys)
-?/. - c.4176C>T r.(?) p.(Ala1392=)
-/. - c.4221C>T r.(?) p.(Ser1407=)
?/. - c.4277G>C r.(?) p.(Gly1426Ala)
?/. - c.4381C>T r.(?) p.(Leu1461Phe)
?/. - c.4389G>C r.(?) p.(Lys1463Asn)
?/. - c.4519A>G r.(?) p.(Ile1507Val)
./. - c.4601C>T r.(?) p.(Pro1534Leu)
?/. - c.4601C>T r.(?) p.(Pro1534Leu)
-/. - c.4640T>C r.(?) p.(Ile1547Thr)
-?/. - c.4640T>C r.(?) p.(Ile1547Thr)
-/. - c.4640T>C r.(?) p.(Ile1547Thr)
?/. - c.4666C>G r.(?) p.(Gln1556Glu)
?/. - c.4730A>C r.(?) p.(Glu1577Ala)
?/. - c.4768G>C r.(?) p.(Val1590Leu)
?/. - c.4859T>C r.(?) p.(Ile1620Thr)
-/. - c.4879T>C r.(?) p.(Leu1627=)
?/. - c.4886C>T r.(?) p.(Ser1629Leu)
?/. - c.4904C>G r.(?) p.(Ala1635Gly)
-?/. - c.4947C>T r.(?) p.(Ser1649=)
?/. - c.4947C>T r.(?) p.(Ser1649=)
?/. - c.4964T>C r.(?) p.(Val1655Ala)
?/. - c.4964T>C r.(?) p.(Val1655Ala)
-?/. - c.5065-4A>G r.spl? p.?
-?/. - c.5157C>T r.(?) p.(Ala1719=)
-?/. - c.5163G>C r.(?) p.(Met1721Ile)
+?/. - c.5201_5224+28del r.spl p.?
-/. - c.5225-10C>A r.(=) p.(=)
-?/. - c.5225-9_5225-8insAT r.(=) p.(=)
-/. - c.5225-7C>T r.(=) p.(=)
-/. - c.5225-6_5225-5del r.spl? p.?
?/. - c.5301A>T r.(?) p.(Glu1767Asp)
?/. - c.5305C>T r.(?) p.(Arg1769Cys)
?/. - c.5324_5325dup r.(?) p.(Ser1776Ter)
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