Transcript #00001409 (NM_006059.3, LAMC3 gene)

Transcript name laminin, gamma 3
Gene name LAMC3 (laminin, gamma 3)
Chromosome 9
Transcript - NCBI ID NM_006059.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_006050.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:31:13 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-2C>T r.(?) p.(=)
-/. - c.75C>T r.(?) p.(Cys25=)
-?/. - c.146A>G r.(?) p.(Gln49Arg)
-/. - c.146A>G r.(?) p.(Gln49Arg)
-?/. - c.146A>G r.(?) p.(Gln49Arg)
?/. - c.178G>T r.(?) p.(Asp60Tyr)
-?/. - c.207C>T r.(?) p.(Gly69=)
-/. - c.219T>G r.(?) p.(His73Gln)
-/. - c.219T>G r.(?) p.(His73Gln)
-?/. - c.290A>G r.(?) p.(Gln97Arg)
-?/. - c.290A>G r.(?) p.(Gln97Arg)
-?/. - c.290A>G r.(?) p.(Gln97Arg)
-?/. - c.290A>G r.(?) p.(Gln97Arg)
?/. - c.309G>T r.(?) p.(Trp103Cys)
?/. - c.364C>G r.(?) p.(Leu122Val)
-/. - c.374-16G>A r.(=) p.(=)
-?/. - c.374-4G>T r.spl? p.?
-/. - c.454C>T r.(?) p.(Arg152Cys)
-/. - c.454C>T r.(?) p.(Arg152Cys)
-/. - c.454C>T r.(?) p.(Arg152Cys)
-?/. - c.454C>T r.(?) p.(Arg152Cys)
-/. - c.454C>T r.(?) p.(Arg152Cys)
-?/. - c.462C>T r.(?) p.(Asp154=)
+?/. 2 c.470G>A r.(?) p.(Trp157*)
?/. - c.514G>A r.(?) p.(Gly172Ser)
-/. - c.521C>A r.(?) p.(Pro174His)
-/. - c.521C>A r.(?) p.(Pro174His)
-/. - c.521_522delinsAG r.(?) p.(Pro174Gln)
-?/. - c.543C>T r.(?) p.(Pro181=)
-?/. - c.558C>T r.(?) p.(Arg186=)
-?/. - c.696C>T r.(?) p.(Thr232=)
-?/. - c.708C>T r.(?) p.(Ile236=)
?/. - c.731T>C r.(?) p.(Phe244Ser)
-/. - c.786G>A r.(?) p.(Val262=)
+?/. - c.809+2_809+8del r.spl p.?
-/. - c.809+13_809+19del r.(=) p.(=)
-?/. - c.835G>A r.(?) p.(Glu279Lys)
-/. - c.855A>G r.(?) p.(Ala285=)
-/. - c.855A>G r.(?) p.(Ala285=)
+?/. 4 c.903_904del r.(?) p.(Cys301*)
-?/. - c.951C>T r.(?) p.(Thr317=)
-/. - c.963C>T r.(?) p.(Ala321=)
-/. - c.963C>T r.(?) p.(Ala321=)
+/. - c.976+1G>A r.spl? p.?
?/. - c.976+1G>C r.spl? p.?
-?/. - c.999C>T r.(?) p.(Ser333=)
-/. - c.1047C>T r.(?) p.(Gly349=)
+?/. 5 c.1048G>A r.(?) p.(Gly350Arg)
?/. - c.1051C>T r.(?) p.(Arg351Cys)
?/. - c.1066C>T r.(?) p.(Arg356Cys)
?/. - c.1115A>G r.(?) p.(Tyr372Cys)
?/. - c.1145C>T r.(?) p.(Pro382Leu)
+?/. 5 c.1156C>T r.(?) p.(Gln386*)
?/. - c.1204G>A r.(?) p.(Ala402Thr)
?/. - c.1218G>A r.(?) p.(=)
-/. - c.1218G>A r.(?) p.(Thr406=)
-/. - c.1218G>A r.(?) p.(Thr406=)
?/. - c.1241G>A r.(?) p.(Arg414His)
?/. - c.1252G>A r.(?) p.(Gly418Arg)
?/. - c.1262C>A r.(?) p.(Ser421*)
-/. - c.1302C>T r.(?) p.(Pro434=)
?/. - c.1330C>T r.(?) p.(Arg444Cys)
?/. - c.1387C>T r.(?) p.(Arg463Cys)
-?/. - c.1411C>A r.(?) p.(Pro471Thr)
-?/. - c.1414C>A r.(?) p.(His472Asn)
-?/. - c.1416C>A r.(?) p.(His472Gln)
-?/. - c.1520-6G>A r.(=) p.(=)
-?/. - c.1520-6G>A r.(=) p.(=)
-/. - c.1526A>C r.(?) p.(Glu509Ala)
-/. - c.1564C>T r.(?) p.(Pro522Ser)
-/. - c.1564C>T r.(?) p.(Pro522Ser)
-/. - c.1631A>G r.(?) p.(Glu544Gly)
-?/. - c.1688G>A r.(?) p.(Arg563Gln)
-?/. - c.1688G>A r.(?) p.(Arg563Gln)
-?/. - c.1699G>A r.(?) p.(Gly567Arg)
?/. - c.1792G>A r.(?) p.(Gly598Arg)
-/. - c.1792G>A r.(?) p.(Gly598Arg)
-/. - c.1823+18T>C r.(=) p.(=)
-?/. - c.1839C>T r.(?) p.(Ser613=)
?/. - c.1865C>G r.(?) p.(Pro622Arg)
-?/. - c.1907G>A r.(?) p.(Arg636His)
-/. - c.1932C>T r.(?) p.(Ser644=)
-/. - c.1932C>T r.(?) p.(Ser644=)
?/. - c.1939G>A r.(?) p.(Gly647Ser)
?/. - c.1939G>A r.(?) p.(Gly647Ser)
?/. - c.1939G>C r.(?) p.(Gly647Arg)
?/. - c.1939G>T r.(?) p.(Gly647Cys)
-/. - c.1939+11A>G r.(=) p.(=)
-/. - c.1939+11A>G r.(=) p.(=)
-/. - c.1940-13del r.(=) p.(=)
-?/. - c.1940-9G>A r.(=) p.(=)
-?/. - c.1994C>T r.(?) p.(Pro665Leu)
-/. - c.2039C>T r.(?) p.(Thr680Met)
-?/. - c.2039C>T r.(?) p.(Thr680Met)
?/. - c.2066C>T r.(?) p.(Pro689Leu)
-/. - c.2066C>T r.(?) p.(Pro689Leu)
-/. - c.2096G>A r.(?) p.(Gly699Asp)
-/. - c.2096G>A r.(?) p.(Gly699Asp)
?/. - c.2227A>G r.(?) p.(Asn743Asp)
-/. - c.2227A>G r.(?) p.(Asn743Asp)
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