Transcript #00010942 (NM_001105206.2, LAMA4 gene)

Transcript name transcript variant 1
Gene name LAMA4 (laminin, alpha 4)
Chromosome 6
Transcript - NCBI ID NM_001105206.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001098676.2
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

672 entries on 7 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.22C>T r.(?) p.(Arg8Cys)
?/. - c.40T>C r.(?) p.(Trp14Arg)
?/. - c.40T>C r.(?) p.(Trp14Arg)
?/. - c.40T>C r.(?) p.(Trp14Arg)
?/. - c.59C>T r.(?) p.(Ala20Val)
?/. - c.67C>T r.(?) p.(Arg23Cys)
-?/. - c.72C>T r.(?) p.(Ala24=)
-/. - c.85G>C r.(?) p.(Asp29His)
-?/. - c.85G>C r.(?) p.(Asp29His)
-?/. - c.85G>T r.(?) p.(Asp29Tyr)
?/. - c.97C>G r.(?) p.(Pro33Ala)
?/. - c.97C>T r.(?) p.(Pro33Ser)
-?/. - c.97C>T r.(?) p.(Pro33Ser)
-?/. - c.106A>G r.(?) p.(Ile36Val)
?/. - c.112G>A r.(?) p.(Gly38Arg)
?/. - c.133del r.(?) p.(Gln45Lysfs*153)
-/. - c.141G>A r.(?) p.(Pro47=)
-/. - c.150G>A r.(?) p.(=)
?/. - c.167C>T r.(?) p.(Ala56Val)
-?/. - c.167C>T r.(?) p.(Ala56Val)
-?/. - c.167C>T r.(?) p.(Ala56Val)
-?/. - c.167C>T r.(?) p.(Ala56Val)
-?/. - c.176G>T r.(?) p.(Arg59Leu)
?/. - c.188C>T r.(?) p.(Ala63Val)
-?/. - c.188C>T r.(?) p.(Ala63Val)
?/. - c.191C>T r.(?) p.(Ala64Val)
-?/. - c.191C>T r.(?) p.(Ala64Val)
?/. - c.195+43C>A r.(=) p.(=)
?/. - c.195+50G>C r.(=) p.(=)
-?/. - c.195+57G>A r.(=) p.(=)
?/. - c.195+71_195+73del r.(=) p.(=)
-?/. - c.195+71_195+73del r.(=) p.(=)
?/. - c.195+71_195+73del r.(=) p.(=)
-?/. - c.195+71_195+73del r.(=) p.(=)
-?/. - c.195+115T>G r.(=) p.(=)
-?/. - c.195+124G>A r.(=) p.(=)
-?/. - c.195+131C>G r.(=) p.(=)
-/. - c.195+131C>G r.(=) p.(=)
-?/. - c.195+142C>T r.(=) p.(=)
-/. - c.195+144T>C r.(=) p.(=)
-/. - c.195+144T>C r.(=) p.(=)
-/. - c.195+144T>C r.(=) p.(=)
-?/. - c.195+144T>C r.(=) p.(=)
-?/. - c.196-15G>C r.(=) p.(=)
-?/. - c.196-15G>C r.(=) p.(=)
-/. - c.196-15G>C r.(=) p.(=)
-?/. - c.196-15G>C r.(=) p.(=)
-/. - c.196-12T>C r.(=) p.(=)
-/. - c.196-12T>C r.(=) p.(=)
-?/. - c.196-12T>C r.(=) p.(=)
-/. - c.196-12T>C r.(=) p.(=)
-/. - c.196-9C>T r.(=) p.(=)
-?/. - c.196-9C>T r.(=) p.(=)
?/. - c.200G>A r.(?) p.(Cys67Tyr)
?/. - c.200G>A r.(?) p.(Cys67Tyr)
?/. - c.200G>A r.(?) p.(Cys67Tyr)
-/. - c.225G>A r.(?) p.(Leu75=)
-?/. - c.225G>A r.(?) p.(Leu75=)
-?/. - c.225G>A r.(?) p.(Leu75=)
?/. - c.227C>T r.(?) p.(Ser76Leu)
-?/. - c.246C>T r.(?) p.(Cys82=)
-?/. - c.254A>G r.(?) p.(Asn85Ser)
-/. - c.264C>T r.(?) p.(Ser88=)
-?/. - c.264C>T r.(?) p.(Ser88=)
-?/. - c.264C>T r.(?) p.(Ser88=)
-/. - c.280G>A r.(?) p.(Gly94Ser)
-/. - c.280G>A r.(?) p.(Gly94Ser)
-/. - c.280G>A r.(?) p.(Gly94Ser)
-/. - c.280G>A r.(?) p.(Gly94Ser)
-/. - c.280G>A r.(?) p.(Gly94Ser)
-?/. - c.297+1G>T r.spl? p.?
-?/. - c.297+8G>A r.(=) p.(=)
-?/. - c.297+8G>A r.(=) p.(=)
-/. - c.297+8G>A r.(=) p.(=)
-/. - c.298-10T>C r.(=) p.(=)
?/. - c.298-2A>G r.spl? p.?
?/. - c.298-2A>G r.spl? p.?
?/. - c.307C>T r.(?) p.(Arg103Trp)
-?/. - c.307C>T r.(?) p.(Arg103Trp)
-?/. - c.307C>T r.(?) p.(Arg103Trp)
-/. - c.309G>A r.(?) p.(Arg103=)
-/. - c.315A>G r.(?) p.(Thr105=)
-?/. - c.349T>C r.(?) p.(Tyr117His)
-?/. - c.349T>C r.(?) p.(Tyr117His)
?/. - c.349T>C r.(?) p.(Tyr117His)
?/. - c.349T>C r.(?) p.(Tyr117His)
?/. - c.354C>G r.(?) p.(Ile118Met)
-?/. - c.354C>T r.(?) p.(Ile118=)
-?/. - c.354C>T r.(?) p.(Ile118=)
?/. - c.355G>A r.(?) p.(Gly119Arg)
?/. - c.364A>G r.(?) p.(Ile122Val)
-?/. - c.411C>A r.(?) p.(Pro137=)
-?/. - c.422+7C>T r.(=) p.(=)
-/. - c.422+20G>C r.(=) p.(=)
-/. - c.422+20G>T r.(=) p.(=)
-/. - c.422+20G>T r.(=) p.(=)
-/. - c.423-10C>T r.(=) p.(=)
-/. - c.423-10C>T r.(=) p.(=)
-/. - c.423-10C>T r.(=) p.(=)
-/. - c.423-10C>T r.(=) p.(=)
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