Transcript #00017762 (NM_002291.2, LAMB1 gene)

Transcript name Manually created transcript. (removed from reference sequence)
Gene name LAMB1 (laminin, beta 1)
Chromosome 7
Transcript - NCBI ID NM_002291.2
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

218 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.38-39C>T 38 r.(=) p.(=) - intron 39
./. - c.468T>C 468 r.(?) p.(=) - coding-synonymous -
./. - c.1135C>T 1135 r.(?) p.(Pro379Ser) - missense -
./. - c.1407G>A 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407G>A 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407G>A 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407G>A 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407G>A 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407G>A 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407G>A 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1407G>A 1407 r.(?) p.(=) - coding-synonymous -
./. - c.1447C>T 1447 r.(?) p.(Arg483Cys) - missense -
./. - c.1447C>T 1447 r.(?) p.(Arg483Cys) - missense -
./. - c.1483-14G>A 1483 r.(=) p.(=) - intron 14
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1776T>G 1776 r.(?) p.(=) - coding-synonymous -
./. - c.1985+12G>A 1985 r.(=) p.(=) - intron 12
./. - c.1985+12G>A 1985 r.(=) p.(=) - intron 12
./. - c.2110-39C>T 2110 r.(=) p.(=) - intron 39
./. - c.2557C>T 2557 r.(?) p.(Arg853Trp) - missense -
./. - c.2578G>A 2578 r.(?) p.(Gly860Ser) - missense -
./. - c.2578G>A 2578 r.(?) p.(Gly860Ser) - missense -
./. - c.2578G>A 2578 r.(?) p.(Gly860Ser) - missense -
./. - c.2578G>A 2578 r.(?) p.(Gly860Ser) - missense -
./. - c.2578G>A 2578 r.(?) p.(Gly860Ser) - missense -
./. - c.2691-18C>T 2691 r.(=) p.(=) - intron 18
./. - c.2723T>C 2723 r.(?) p.(Ile908Thr) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3065A>G 3065 r.(?) p.(Gln1022Arg) - missense -
./. - c.3141C>T 3141 r.(?) p.(=) - coding-synonymous -
./. - c.3141C>T 3141 r.(?) p.(=) - coding-synonymous -
./. - c.3300G>C 3300 r.(?) p.(=) - coding-synonymous -
./. - c.3300G>C 3300 r.(?) p.(=) - coding-synonymous -
./. - c.3342C>T 3342 r.(?) p.(=) - coding-synonymous -
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
./. - c.3392-36T>C 3392 r.(=) p.(=) - intron 36
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