Transcript #00029713 (NM_001014980.2, FAM132A gene)

Transcript name family with sequence similarity 132, member A
Gene name FAM132A (family with sequence similarity 132, member A)
Chromosome 1
Transcript - NCBI ID NM_001014980.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001014980.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

44 entries on 1 page. Showing entries 1 - 44.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.379+16C>G 379 r.(=) p.(=) - intron 16
./. - c.379+39G>A 379 r.(=) p.(=) - intron 39
./. - c.480T>C 480 r.(?) p.(=) - coding-synonymous -
./. - c.480T>C 480 r.(?) p.(=) - coding-synonymous -
./. - c.480T>C 480 r.(?) p.(=) - coding-synonymous -
./. - c.531+25C>T 531 r.(=) p.(=) - intron 25
./. - c.531+25C>T 531 r.(=) p.(=) - intron 25
./. - c.531+25C>T 531 r.(=) p.(=) - intron 25
./. - c.531+25C>T 531 r.(=) p.(=) - intron 25
./. - c.531+25C>T 531 r.(=) p.(=) - intron 25
./. - c.531+25C>T 531 r.(=) p.(=) - intron 25
./. - c.531+25C>T 531 r.(=) p.(=) - intron 25
./. - c.531+25C>T 531 r.(=) p.(=) - intron 25
./. - c.532-3C>T 532 r.spl? p.? - splice 3
./. - c.539C>T 539 r.(?) p.(Ala180Val) - missense -
./. - c.539C>T 539 r.(?) p.(Ala180Val) - missense -
./. - c.539C>T 539 r.(?) p.(Ala180Val) - missense -
./. - c.539C>T 539 r.(?) p.(Ala180Val) - missense -
./. - c.539C>T 539 r.(?) p.(Ala180Val) - missense -
./. - c.539C>T 539 r.(?) p.(Ala180Val) - missense -
./. - c.539C>T 539 r.(?) p.(Ala180Val) - missense -
./. - c.691T>C 691 r.(?) p.(Cys231Arg) - missense -
./. - c.691T>C 691 r.(?) p.(Cys231Arg) - missense -
./. - c.691T>C 691 r.(?) p.(Cys231Arg) - missense -
./. - c.691T>C 691 r.(?) p.(Cys231Arg) - missense -
./. - c.691T>C 691 r.(?) p.(Cys231Arg) - missense -
./. - c.691T>C 691 r.(?) p.(Cys231Arg) - missense -
./. - c.691T>C 691 r.(?) p.(Cys231Arg) - missense -
./. - c.691T>C 691 r.(?) p.(Cys231Arg) - missense -
./. - c.691T>C 691 r.(?) p.(Cys231Arg) - missense -
./. - c.691T>C 691 r.(?) p.(Cys231Arg) - missense -
./. - c.720C>T 720 r.(?) p.(=) - coding-synonymous -
./. - c.759G>A 759 r.(?) p.(=) - coding-synonymous -
./. - c.780G>A 780 r.(?) p.(=) - coding-synonymous -
./. - c.780G>A 780 r.(?) p.(=) - coding-synonymous -
./. - c.780G>A 780 r.(?) p.(=) - coding-synonymous -
./. - c.780G>A 780 r.(?) p.(=) - coding-synonymous -
./. - c.780G>A 780 r.(?) p.(=) - coding-synonymous -
./. - c.780G>A 780 r.(?) p.(=) - coding-synonymous -
./. - c.780G>A 780 r.(?) p.(=) - coding-synonymous -
./. - c.*9delA 918 r.(=) p.(=) - utr-3 -
./. - c.*9delA 918 r.(=) p.(=) - utr-3 -
./. - c.*35G>A 944 r.(=) p.(=) - utr-3 -
./. - c.*35G>A 944 r.(=) p.(=) - utr-3 -
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