Transcript #00017756 (NM_001127718.1, LAMA3 gene)

Transcript name Manually created transcript. (removed from reference sequence)
Gene name LAMA3 (laminin, alpha 3)
Chromosome 18
Transcript - NCBI ID NM_001127718.1
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.84C>T 84 r.(?) p.(=) - coding-synonymous -
./. - c.84C>T 84 r.(?) p.(=) - coding-synonymous -
./. - c.84C>T 84 r.(?) p.(=) - coding-synonymous -
./. - c.495C>T 495 r.(?) p.(=) - coding-synonymous -
./. - c.495C>T 495 r.(?) p.(=) - coding-synonymous -
./. - c.495C>T 495 r.(?) p.(=) - coding-synonymous -
./. - c.495C>T 495 r.(?) p.(=) - coding-synonymous -
./. - c.495C>T 495 r.(?) p.(=) - coding-synonymous -
./. - c.495C>T 495 r.(?) p.(=) - coding-synonymous -
./. - c.495C>T 495 r.(?) p.(=) - coding-synonymous -
./. - c.635-44G>A 635 r.(=) p.(=) - intron 44
./. - c.635-44G>A 635 r.(=) p.(=) - intron 44
./. - c.635-44G>A 635 r.(=) p.(=) - intron 44
./. - c.635-44G>A 635 r.(=) p.(=) - intron 44
./. - c.635-44G>A 635 r.(=) p.(=) - intron 44
./. - c.635-44G>A 635 r.(=) p.(=) - intron 44
./. - c.635-44G>A 635 r.(=) p.(=) - intron 44
./. - c.635-44G>A 635 r.(=) p.(=) - intron 44
./. - c.635-44G>A 635 r.(=) p.(=) - intron 44
./. - c.635-44G>A 635 r.(=) p.(=) - intron 44
./. - c.635-44G>A 635 r.(=) p.(=) - intron 44
./. - c.635-44G>A 635 r.(=) p.(=) - intron 44
./. - c.1152C>G 1152 r.(?) p.(=) - coding-synonymous -
./. - c.1152C>G 1152 r.(?) p.(=) - coding-synonymous -
./. - c.1152C>G 1152 r.(?) p.(=) - coding-synonymous -
./. - c.1152C>G 1152 r.(?) p.(=) - coding-synonymous -
./. - c.1152C>G 1152 r.(?) p.(=) - coding-synonymous -
./. - c.1152C>G 1152 r.(?) p.(=) - coding-synonymous -
./. - c.1152C>G 1152 r.(?) p.(=) - coding-synonymous -
./. - c.1479-36G>A 1479 r.(=) p.(=) - intron 36
./. - c.1560C>T 1560 r.(?) p.(=) - coding-synonymous -
./. - c.1560C>T 1560 r.(?) p.(=) - coding-synonymous -
./. - c.1560C>T 1560 r.(?) p.(=) - coding-synonymous -
./. - c.1560C>T 1560 r.(?) p.(=) - coding-synonymous -
./. - c.1560C>T 1560 r.(?) p.(=) - coding-synonymous -
./. - c.1872G>A 1872 r.(?) p.(=) - coding-synonymous -
./. - c.2566G>A 2566 r.(?) p.(Asp856Asn) - missense -
./. - c.2652T>C 2652 r.(?) p.(=) - coding-synonymous-near-splice -
./. - c.3109A>G 3109 r.(?) p.(Thr1037Ala) - missense -
./. - c.3109A>G 3109 r.(?) p.(Thr1037Ala) - missense -
./. - c.3450C>A 3450 r.(?) p.(Asn1150Lys) - missense -
./. - c.3450C>A 3450 r.(?) p.(Asn1150Lys) - missense -
./. - c.3450C>A 3450 r.(?) p.(Asn1150Lys) - missense -
./. - c.3450C>A 3450 r.(?) p.(Asn1150Lys) - missense -
./. - c.3450C>A 3450 r.(?) p.(Asn1150Lys) - missense -
./. - c.3450C>A 3450 r.(?) p.(Asn1150Lys) - missense -
./. - c.3450C>A 3450 r.(?) p.(Asn1150Lys) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3505A>G 3505 r.(?) p.(Ser1169Gly) - missense -
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
./. - c.3581+7G>C 3581 r.(=) p.(=) - splice 7
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