Transcript #00012263 (NM_001145808.1, ITGAM gene)

Transcript name transcript variant 1
Gene name ITGAM (integrin, alpha M (complement component 3 receptor 3 subunit))
Chromosome 16
Transcript - NCBI ID NM_001145808.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001139280.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

135 entries on 2 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.-38C>T -38 r.(=) p.(=) - utr-5 -
./. - c.-38C>T -38 r.(=) p.(=) - utr-5 -
./. - c.-38C>T -38 r.(=) p.(=) - utr-5 -
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.134+11T>C 134 r.(=) p.(=) - intron 11
./. - c.230G>A 230 r.(?) p.(Arg77His) - missense -
./. - c.230G>A 230 r.(?) p.(Arg77His) - missense -
./. - c.230G>A 230 r.(?) p.(Arg77His) - missense -
./. - c.230G>A 230 r.(?) p.(Arg77His) - missense -
./. - c.559-4G>A 559 r.spl? p.? - splice 4
./. - c.559-4G>A 559 r.spl? p.? - splice 4
./. - c.559-4G>A 559 r.spl? p.? - splice 4
./. - c.559-4G>A 559 r.spl? p.? - splice 4
./. - c.704+10C>G 704 r.(=) p.(=) - intron 10
./. - c.704+10C>G 704 r.(=) p.(=) - intron 10
./. - c.704+10C>G 704 r.(=) p.(=) - intron 10
./. - c.704+10C>G 704 r.(=) p.(=) - intron 10
./. - c.704+10C>G 704 r.(=) p.(=) - intron 10
./. - c.704+10C>G 704 r.(=) p.(=) - intron 10
./. - c.1322T>C 1322 r.(?) p.(Met441Thr) - missense -
./. - c.1322T>C 1322 r.(?) p.(Met441Thr) - missense -
./. - c.1322T>C 1322 r.(?) p.(Met441Thr) - missense -
./. - c.1322T>C 1322 r.(?) p.(Met441Thr) - missense -
./. - c.1569A>T 1569 r.(?) p.(=) - coding-synonymous -
./. - c.1804C>T 1804 r.(?) p.(=) - coding-synonymous -
./. - c.1804C>T 1804 r.(?) p.(=) - coding-synonymous -
./. - c.1804C>T 1804 r.(?) p.(=) - coding-synonymous -
./. - c.1947C>T 1947 r.(?) p.(=) - coding-synonymous -
./. - c.2160+32T>C 2160 r.(=) p.(=) - intron 32
./. - c.2160+32T>C 2160 r.(=) p.(=) - intron 32
./. - c.2160+32T>C 2160 r.(=) p.(=) - intron 32
./. - c.2160+32T>C 2160 r.(=) p.(=) - intron 32
./. - c.2160+32T>C 2160 r.(=) p.(=) - intron 32
./. - c.2160+32T>C 2160 r.(=) p.(=) - intron 32
./. - c.2160+32T>C 2160 r.(=) p.(=) - intron 32
./. - c.2160+32T>C 2160 r.(=) p.(=) - intron 32
./. - c.2160+32T>C 2160 r.(=) p.(=) - intron 32
./. - c.2160+32T>C 2160 r.(=) p.(=) - intron 32
./. - c.2160+32T>C 2160 r.(=) p.(=) - intron 32
./. - c.2366+37_2366+48del 2366 r.(=) p.(=) - intron 37
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2502G>A 2502 r.(?) p.(=) - coding-synonymous -
./. - c.2576C>T 2576 r.(?) p.(Ala859Val) - missense -
./. - c.2576C>T 2576 r.(?) p.(Ala859Val) - missense -
./. - c.2576C>T 2576 r.(?) p.(Ala859Val) - missense -
./. - c.2576C>T 2576 r.(?) p.(Ala859Val) - missense -
./. - c.2576C>T 2576 r.(?) p.(Ala859Val) - missense -
./. - c.2576C>T 2576 r.(?) p.(Ala859Val) - missense -
./. - c.2576C>T 2576 r.(?) p.(Ala859Val) - missense -
./. - c.2796-29C>T 2796 r.(=) p.(=) - intron 29
./. - c.2796-29C>T 2796 r.(=) p.(=) - intron 29
./. - c.3390+12T>C 3390 r.(=) p.(=) - intron 12
./. - c.3390+12T>C 3390 r.(=) p.(=) - intron 12
./. - c.3390+12T>C 3390 r.(=) p.(=) - intron 12
./. - c.3390+12T>C 3390 r.(=) p.(=) - intron 12
./. - c.3390+12T>C 3390 r.(=) p.(=) - intron 12
./. - c.3390+12T>C 3390 r.(=) p.(=) - intron 12
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