Transcript #00025347 (NM_198129.1, LAMA3 gene)

Transcript name transcript variant 1
Gene name LAMA3 (laminin, alpha 3)
Chromosome 18
Transcript - NCBI ID NM_198129.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_937762.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -


Variants

69 entries on 1 page. Showing entries 1 - 69.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.57G>C r.(?) p.(Thr19=)
-/. - c.295-4del r.spl? p.?
?/. - c.813C>G r.(?) p.(His271Gln)
-?/. - c.856-9G>C r.(=) p.(=)
-?/. - c.891G>A r.(?) p.(Gly297=)
?/. - c.1273+26_1273+41del r.(=) p.(=)
?/. - c.1636A>G r.(?) p.(Met546Val)
-?/. - c.1788+19G>C r.(=) p.(=)
+?/. - c.1789-7_1789-5del r.(?) p.?
-?/. - c.1806G>A r.(?) p.(Lys602=)
?/. - c.1813G>A r.(?) p.(Val605Ile)
-?/. - c.1889-9T>C r.(=) p.(=)
?/. - c.2466T>A r.(?) p.(Ser822Arg)
-?/. - c.2571+8T>G r.(=) p.(=)
?/. - c.2585T>C r.(?) p.(Leu862Pro)
-?/. - c.2874T>G r.(?) p.(Val958=)
-/. - c.2901T>C r.(?) p.(Ala967=)
-?/. - c.3615A>G r.(?) p.(Leu1205=)
?/. - c.3622C>A r.(?) p.(Pro1208Thr)
-?/. - c.4029C>T r.(?) p.(His1343=)
-?/. - c.4060G>A r.(?) p.(Glu1354Lys)
-?/. - c.4110G>A r.(?) p.(Glu1370=)
?/. - c.4163A>T r.(?) p.(Gln1388Leu)
?/. - c.4226G>T r.(?) p.(Arg1409Ile)
-/. - c.4260G>C r.(?) p.(Gly1420=)
?/. - c.4432A>T r.(?) p.(Met1478Leu)
-/. - c.4530C>T r.(?) p.(Pro1510=)
-?/. - c.4584+14G>A r.(=) p.(=)
-?/. - c.4643A>G r.(?) p.(Asp1548Gly)
-?/. - c.4758C>T r.(?) p.(His1586=)
?/. - c.4998+1421G>T r.(=) p.(=)
?/. - c.5068A>G r.(?) p.(Asn1690Asp)
?/. - c.5512G>A r.(?) p.(Glu1838Lys)
-?/. - c.5522G>T r.(?) p.(Arg1841Leu)
+/. - c.5904dup r.(?) p.(Glu1969ArgfsTer4)
+?/. - c.6115C>T r.(?) p.(Arg2039Cys)
?/. - c.6122G>A r.(?) p.(Arg2041Gln)
+/. - c.6477_6486del r.(?) p.(Ile2159MetfsTer46)
-?/. - c.6525C>T r.(?) p.(Ala2175=)
+/. - c.6745C>T r.(?) p.(Gln2249Ter)
+/. - c.6960T>A r.(?) p.(Tyr2320*)
-?/. - c.6985A>G r.(?) p.(Lys2329Glu)
-?/. - c.7218C>T r.(?) p.(Asp2406=)
-?/. - c.7545C>T r.(?) p.(Pro2515=)
+/. - c.7737_7738del r.(?) p.(Lys2579AsnfsTer8)
?/. - c.7742T>C r.(?) p.(Phe2581Ser)
-/. - c.7797C>T r.(?) p.(Asp2599=)
+?/. - c.8043G>A r.(?) p.(Ser2681=)
?/. - c.8445C>A r.(?) p.(Asn2815Lys)
-?/. - c.8497G>A r.(?) p.(Gly2833Ser)
-/. - c.8500A>G r.(?) p.(Ser2834Gly)
?/. - c.8566G>A r.(?) p.(Asp2856Asn)
-/. - c.8576+7G>C r.(=) p.(=)
-?/. - c.8576+7G>T r.(=) p.(=)
-?/. - c.8576+7G>T r.(=) p.(=)
-?/. - c.8708+4G>A r.spl? p.?
./. - c.8851C>T r.(?) p.(Arg2951Cys)
-?/. - c.8851C>T r.(?) p.(Arg2951Cys)
-?/. - c.8898C>T r.(=) p.(=)
?/. - c.9067G>A r.(?) p.(Gly3023Arg)
?/. - c.9269G>T r.(?) p.(Arg3090Leu)
-/. - c.9352-7G>A r.(=) p.(=)
-?/. - c.9353G>A r.(?) p.(Ser3118Asn)
-?/. - c.9353G>A r.(?) p.(Ser3118Asn)
?/. - c.9500A>C r.(?) p.(His3167Pro)
+/. - c.9511+1G>A r.spl? p.?
-?/. - c.9512-4A>T r.spl? p.?
-?/. - c.9559C>T r.(?) p.(Arg3187Cys)
-/. - c.9643-14C>T r.(=) p.(=)
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