Transcript #00010939 (NM_005559.3, LAMA1 gene)

Transcript name laminin, alpha 1
Gene name LAMA1 (laminin, alpha 1)
Chromosome 18
Transcript - NCBI ID NM_005559.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_005550.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

344 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.10_11delinsC r.(?) p.(Gly4ProfsTer83)
+?/. - c.62-3C>G r.spl? p.?
+?/. 2 c.164A>T r.(?) p.(His55Leu)
?/. - c.176G>A r.(?) p.(Arg59Gln)
-?/. - c.181G>A r.(?) p.(Val61Ile)
-?/. - c.181G>A r.(?) p.(Val61Ile)
-?/. - c.327C>T r.(?) p.(Ile109=)
+/. 3i_11i c.(345+1_346-1)_(1563+1_1564-1)del r.346_1563del p.Phe117_Val522del
?/. - c.362_363del r.(?) p.(Tyr121CysfsTer4)
?/. - c.371T>C r.(?) p.(Ile124Thr)
?/. - c.371T>C r.(?) p.(Ile124Thr)
?/. - c.371T>C r.(?) p.(Ile124Thr)
-?/. - c.421C>T r.(?) p.(Leu141=)
+?/. 4 c.470C>G r.(?) p.(Ser157*)
?/. - c.484C>T r.(?) p.(Arg162Cys)
?/. - c.493A>G r.(?) p.(Ile165Val)
+/. 4 c.555T>G r.(?) p.(Tyr185*)
+/. 4i c.588+2T>G r.spl? p.?
?/. - c.628G>A r.(?) p.(Asp210Asn)
+/. - c.628_637del r.(?) p.(Asp210ProfsTer27)
?/. - c.665G>A r.(?) p.(Arg222Gln)
-?/. - c.674G>A r.(?) p.(Arg225His)
?/. - c.680G>A r.(?) p.(Arg227His)
?/. - c.680G>A r.(?) p.(Arg227His)
?/. - c.731G>A r.(?) p.(Arg244Gln)
-?/. - c.745C>G r.(?) p.(Leu249Val)
?/. - c.756del r.(?) p.(Ile252MetfsTer10)
+/. 5i c.768+1G>A r.spl? p.?
-?/. - c.840A>G r.(?) p.(Pro280=)
+/. - c.842G>A r.(?) p.(Trp281Ter)
+/. - c.842G>A r.(?) p.(Trp281Ter)
+?/. - c.858+1G>T r.spl? p.?
+/. - c.858+1G>T r.spl? p.?
-?/. - c.859-4G>A r.spl? p.?
?/. - c.923A>C r.(?) p.(Tyr308Ser)
?/. - c.935C>T r.(?) p.(Pro312Leu)
?/. - c.944C>T r.(?) p.(Pro315Leu)
-?/. - c.977-19G>A r.(=) p.(=)
?/. - c.1013A>G r.(?) p.(Tyr338Cys)
-?/. - c.1156-9G>A r.(=) p.(=)
?/. - c.1183C>T r.(?) p.(Arg395Cys)
?/. - c.1274G>C r.(?) p.(Gly425Ala)
?/. - c.1277A>G r.(?) p.(Gln426Arg)
?/. - c.1294G>T r.(?) p.(Gly432Cys)
+?/. 33 c.1404_1405del r.(?) p.(Gly469Alafs*5)
-?/. - c.1563+9C>T r.(=) p.(=)
-?/. - c.1563+9C>T r.(=) p.(=)
-/. - c.1563+23_1563+25dup r.(=) p.(=)
-?/. - c.1619C>T r.(?) p.(Pro540Leu)
-?/. - c.1631A>G r.(?) p.(Asp544Gly)
-?/. - c.1673C>T r.(?) p.(Ala558Val)
?/. - c.1714C>A r.(?) p.(Pro572Thr)
-?/. - c.1716C>T r.(?) p.(Pro572=)
./. - c.1730G>C r.(?) p.(Gly577Ala)
?/. - c.1745C>T r.(?) p.(Ala582Val)
-?/. - c.1746G>A r.(?) p.(Ala582=)
+?/. 13 c.1774_1775insTTCATAAT r.(?) p.(Ser592Phefs*9)
-/. - c.1784T>C r.(?) p.(Ile595Thr)
-?/. - c.1788G>A r.(?) p.(Pro596=)
?/. - c.1792G>C r.(?) p.(Glu598Gln)
-/. - c.1803C>T r.(?) p.(Asp601=)
-/. - c.1803C>T r.(?) p.(Asp601=)
?/. - c.1862C>T r.(?) p.(Thr621Ile)
?/. - c.1877T>A r.(?) p.(Leu626Gln)
?/. - c.2027A>G r.(?) p.(Asn676Ser)
-?/. - c.2030C>T r.(?) p.(Ser677Phe)
?/. - c.2030C>T r.(?) p.(Ser677Phe)
-/. - c.2052-18C>A r.(=) p.(=)
+?/. 15 c.2108C>T r.(?) p.(Ala703Val)
?/. - c.2108C>T r.(?) p.(Ala703Val)
-?/. - c.2136G>T r.(?) p.(Pro712=)
-?/. - c.2136G>T r.(?) p.(Pro712=)
-?/. - c.2139A>G r.(?) p.(Gln713=)
-?/. - c.2164-7C>T r.(=) p.(=)
-?/. - c.2186G>A r.(?) p.(Arg729His)
-?/. - c.2186G>A r.(?) p.(Arg729His)
?/. - c.2199A>G r.(?) p.(Ile733Met)
-?/. - c.2257G>A r.(?) p.(Val753Ile)
-?/. - c.2262C>T r.(?) p.(His754=)
-?/. - c.2275-10A>G r.(=) p.(=)
-?/. - c.2277G>A r.(?) p.(Ala759=)
?/. - c.2279G>C r.(?) p.(Cys760Ser)
?/. - c.2293A>G r.(?) p.(Thr765Ala)
-?/. - c.2295C>T r.(?) p.(Thr765=)
-?/. - c.2299G>A r.(?) p.(Val767Ile)
-?/. - c.2331C>T r.(?) p.(Tyr777=)
-?/. - c.2389A>G r.(?) p.(Ile797Val)
-?/. - c.2453G>C r.(?) p.(Trp818Ser)
-?/. - c.2462C>A r.(?) p.(Pro821Gln)
-?/. - c.2469C>T r.(?) p.(Tyr823=)
?/. - c.2515C>T r.(?) p.(Pro839Ser)
?/. - c.2515C>T r.(?) p.(Pro839Ser)
?/. - c.2524C>T r.(?) p.(Pro842Ser)
?/. - c.2524C>T r.(?) p.(Pro842Ser)
?/. - c.2527G>A r.(?) p.(Gly843Ser)
?/. - c.2557G>A r.(?) p.(Gly853Ser)
-?/. - c.2562C>T r.(?) p.(Asn854=)
+?/. 19 c.2616del r.(?) p.(Lys872Asnfs*23)
-?/. - c.2657C>T r.(?) p.(Ala886Val)
?/. - c.2657C>T r.(?) p.(Ala886Val)
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