Transcript #00017905 (NM_001173498.1, MAN2B1 gene)

Transcript name Manually created transcript. (removed from reference sequence)
Gene name MAN2B1 (mannosidase, alpha, class 2B, member 1)
Chromosome 19
Transcript - NCBI ID NM_001173498.1
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

174 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.-4213G>A -4213 r.(=) p.(=) - utr-5 -
./. - c.-4213G>A -4213 r.(=) p.(=) - utr-5 -
./. - c.-3843C>T -3843 r.(=) p.(=) - utr-5 -
./. - c.-3843C>T -3843 r.(=) p.(=) - utr-5 -
./. - c.-3843C>T -3843 r.(=) p.(=) - utr-5 -
./. - c.-3843C>T -3843 r.(=) p.(=) - utr-5 -
./. - c.-3843C>T -3843 r.(=) p.(=) - utr-5 -
./. - c.-3198G>A -3198 r.(=) p.(=) - utr-5 -
./. - c.-3034C>G -3034 r.(=) p.(=) - utr-5 -
./. - c.-3034C>G -3034 r.(=) p.(=) - utr-5 -
./. - c.-2664C>T -2664 r.(=) p.(=) - utr-5 -
./. - c.-2664C>T -2664 r.(=) p.(=) - utr-5 -
./. - c.-2664C>T -2664 r.(=) p.(=) - utr-5 -
./. - c.-2639C>T -2639 r.(=) p.(=) - utr-5 -
./. - c.-2639C>T -2639 r.(=) p.(=) - utr-5 -
./. - c.-2639C>T -2639 r.(=) p.(=) - utr-5 -
./. - c.-2639C>T -2639 r.(=) p.(=) - utr-5 -
./. - c.-2639C>T -2639 r.(=) p.(=) - utr-5 -
./. - c.-2639C>T -2639 r.(=) p.(=) - utr-5 -
./. - c.-2639C>T -2639 r.(=) p.(=) - utr-5 -
./. - c.-2639C>T -2639 r.(=) p.(=) - utr-5 -
./. - c.-2639C>T -2639 r.(=) p.(=) - utr-5 -
./. - c.-2639C>T -2639 r.(=) p.(=) - utr-5 -
./. - c.-2639C>T -2639 r.(=) p.(=) - utr-5 -
./. - c.-1655C>T -1655 r.(=) p.(=) - utr-5 -
./. - c.-1655C>T -1655 r.(=) p.(=) - utr-5 -
./. - c.-1655C>T -1655 r.(=) p.(=) - utr-5 -
./. - c.-1655C>T -1655 r.(=) p.(=) - utr-5 -
./. - c.-1655C>T -1655 r.(=) p.(=) - utr-5 -
./. - c.436+34C>T 436 r.(=) p.(=) - intron 34
./. - c.437-37C>T 437 r.(=) p.(=) - intron 37
./. - c.437-37C>T 437 r.(=) p.(=) - intron 37
./. - c.437-37C>T 437 r.(=) p.(=) - intron 37
./. - c.437-37C>T 437 r.(=) p.(=) - intron 37
./. - c.747C>T 747 r.(?) p.(=) - coding-synonymous -
./. - c.747C>T 747 r.(?) p.(=) - coding-synonymous -
./. - c.747C>T 747 r.(?) p.(=) - coding-synonymous -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.832C>G 832 r.(?) p.(Leu278Val) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.935C>T 935 r.(?) p.(Thr312Ile) - missense -
./. - c.1010G>A 1010 r.(?) p.(Arg337Gln) - missense -
./. - c.1010G>A 1010 r.(?) p.(Arg337Gln) - missense -
./. - c.1010G>A 1010 r.(?) p.(Arg337Gln) - missense -
./. - c.1010G>A 1010 r.(?) p.(Arg337Gln) - missense -
./. - c.1010G>A 1010 r.(?) p.(Arg337Gln) - missense -
./. - c.1010G>A 1010 r.(?) p.(Arg337Gln) - missense -
./. - c.1010G>A 1010 r.(?) p.(Arg337Gln) - missense -
./. - c.1010G>A 1010 r.(?) p.(Arg337Gln) - missense -
./. - c.1010G>A 1010 r.(?) p.(Arg337Gln) - missense -
./. - c.1010G>A 1010 r.(?) p.(Arg337Gln) - missense -
./. - c.1235A>G 1235 r.(?) p.(Asn412Ser) - missense -
./. - c.1235A>G 1235 r.(?) p.(Asn412Ser) - missense -
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1306+34C>A 1306 r.(=) p.(=) - intron 34
./. - c.1307-22C>T 1307 r.(=) p.(=) - intron 22
./. - c.1307-22C>T 1307 r.(=) p.(=) - intron 22
./. - c.1307-22C>T 1307 r.(=) p.(=) - intron 22
./. - c.1307-22C>T 1307 r.(=) p.(=) - intron 22
./. - c.1307-22C>T 1307 r.(=) p.(=) - intron 22
./. - c.1307-22C>T 1307 r.(=) p.(=) - intron 22
./. - c.1307-22C>T 1307 r.(=) p.(=) - intron 22
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