Transcript #00012264 (NM_000632.3, ITGAM gene)

Transcript name transcript variant 2
Gene name ITGAM (integrin, alpha M (complement component 3 receptor 3 subunit))
Chromosome 16
Transcript - NCBI ID NM_000632.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000623.2
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.1566A>T 1566 r.(?) p.(=) - coding-synonymous -
./. - c.1801C>T 1801 r.(?) p.(=) - coding-synonymous -
./. - c.1801C>T 1801 r.(?) p.(=) - coding-synonymous -
./. - c.1801C>T 1801 r.(?) p.(=) - coding-synonymous -
./. - c.1944C>T 1944 r.(?) p.(=) - coding-synonymous -
./. - c.2157+32T>C 2157 r.(=) p.(=) - intron 32
./. - c.2157+32T>C 2157 r.(=) p.(=) - intron 32
./. - c.2157+32T>C 2157 r.(=) p.(=) - intron 32
./. - c.2157+32T>C 2157 r.(=) p.(=) - intron 32
./. - c.2157+32T>C 2157 r.(=) p.(=) - intron 32
./. - c.2157+32T>C 2157 r.(=) p.(=) - intron 32
./. - c.2157+32T>C 2157 r.(=) p.(=) - intron 32
./. - c.2157+32T>C 2157 r.(=) p.(=) - intron 32
./. - c.2157+32T>C 2157 r.(=) p.(=) - intron 32
./. - c.2157+32T>C 2157 r.(=) p.(=) - intron 32
./. - c.2157+32T>C 2157 r.(=) p.(=) - intron 32
./. - c.2363+37_2363+48del 2363 r.(=) p.(=) - intron 37
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2499G>A 2499 r.(?) p.(=) - coding-synonymous -
./. - c.2573C>T 2573 r.(?) p.(Ala858Val) - missense -
./. - c.2573C>T 2573 r.(?) p.(Ala858Val) - missense -
./. - c.2573C>T 2573 r.(?) p.(Ala858Val) - missense -
./. - c.2573C>T 2573 r.(?) p.(Ala858Val) - missense -
./. - c.2573C>T 2573 r.(?) p.(Ala858Val) - missense -
./. - c.2573C>T 2573 r.(?) p.(Ala858Val) - missense -
./. - c.2573C>T 2573 r.(?) p.(Ala858Val) - missense -
./. - c.2793-29C>T 2793 r.(=) p.(=) - intron 29
./. - c.2793-29C>T 2793 r.(=) p.(=) - intron 29
./. - c.3387+12T>C 3387 r.(=) p.(=) - intron 12
./. - c.3387+12T>C 3387 r.(=) p.(=) - intron 12
./. - c.3387+12T>C 3387 r.(=) p.(=) - intron 12
./. - c.3387+12T>C 3387 r.(=) p.(=) - intron 12
./. - c.3387+12T>C 3387 r.(=) p.(=) - intron 12
./. - c.3387+12T>C 3387 r.(=) p.(=) - intron 12
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