Transcript #00007885 (NM_031471.5, FERMT3 gene)

Transcript name transcript variant URP2SF
Gene name FERMT3 (fermitin family member 3)
Chromosome 11
Transcript - NCBI ID NM_031471.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_113659.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

139 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-14-8C>T r.(=) p.(=)
?/. - c.-14-6C>T r.(=) p.(=)
-?/. - c.-14-6_-14-5del r.spl? p.?
+/. - c.48G>A r.(?) p.(Trp16Ter)
+/. - c.48G>A r.(?) p.(Trp16Ter)
-/. - c.119C>T r.(?) p.(Ser40Leu)
+/. - c.126del r.(?) p.(Ile42MetfsTer6)
+/. - c.126del r.(?) p.(Ile42MetfsTer6)
-?/. - c.130G>A r.(?) p.(Gly44Arg)
-/. - c.130G>A r.(?) p.(Gly44Arg)
-/. - c.130G>A r.(?) p.(Gly44Arg)
-?/. - c.159C>G r.(?) p.(Ile53Met)
?/. - c.159C>G r.(?) p.(Ile53Met)
-?/. - c.159C>G r.(?) p.(Ile53Met)
-/. - c.161-11G>A r.(=) p.(=)
+/. - c.161-2A>C r.spl p.?
-?/. - c.201A>G r.(?) p.(Glu67=)
+/. - c.238_244dup r.(?) p.(Lys82ThrfsTer67)
-/. - c.249C>T r.(?) p.(Tyr83=)
?/. - c.268C>T r.(?) p.(Arg90Cys)
-?/. - c.268C>T r.(?) p.(Arg90Cys)
+/. - c.286C>T r.(?) p.(Gln96Ter)
+/. - c.305T>C r.(?) p.(Leu102Pro)
?/. - c.332G>A r.(?) p.(Arg111His)
?/. - c.332G>A r.(?) p.(Arg111His)
?/. - c.332G>A r.(?) p.(Arg111His)
?/. - c.332G>A r.(?) p.(Arg111His)
-/. - c.405C>T r.(?) p.(His135=)
-?/. - c.456_458del r.(?) p.(Lys153del)
-?/. - c.515-20A>T r.(=) p.(=)
-?/. - c.515-8C>A r.(=) p.(=)
-?/. - c.515-5T>A r.spl? p.?
-?/. - c.515-5T>A r.spl? p.?
-/. - c.527C>T r.(?) p.(Ala176Val)
-?/. - c.527C>T r.(?) p.(Ala176Val)
-?/. - c.527C>T r.(?) p.(Ala176Val)
-?/. - c.568C>G r.(?) p.(Gln190Glu)
?/. - c.608C>T r.(?) p.(Pro203Leu)
-?/. - c.615C>T r.(?) p.(Pro205=)
-?/. - c.615C>T r.(?) p.(Pro205=)
-?/. - c.615C>T r.(?) p.(Pro205=)
-?/. - c.683+18G>A r.(=) p.(=)
-/. - c.684-5C>G r.(?) p.(=)
-?/. - c.684-5C>G r.spl? p.?
+/. - c.687G>A r.(?) p.(Trp229Ter)
+/. - c.687G>A r.(?) p.(Trp229Ter)
+/. - c.687G>A r.(?) p.(Trp229Ter)
+/. - c.687G>A r.(?) p.(Trp229Ter)
+/. - c.687G>A r.(?) p.(Trp229Ter)
+/. - c.687G>T r.(?) p.(Trp229Cys)
+/. - c.687G>T r.(?) p.(Trp229Cys)
-?/. - c.696G>A r.(?) p.(Ser232=)
-/. - c.729C>T r.(?) p.(Ala243=)
-/. - c.729C>T r.(?) p.(Ala243=)
-/. - c.736G>A r.(?) p.(Ala246Thr)
+/. - c.756G>C r.(?) p.(Lys252Asn)
-/. - c.787-10C>A r.(=) p.(=)
-?/. - c.787-8C>G r.(=) p.(=)
+/. - c.821A>G r.(?) p.(Gln274Arg)
+/. - c.830G>A r.(?) p.(Trp277Ter)
+/. - c.873G>A r.(?) p.(Met291Ile)
-/. - c.895-4C>T r.(?) p.(=)
-/. - c.895-4C>T r.spl? p.?
+/. - c.895-3T>G r.spl p.?
-?/. - c.921C>T r.(?) p.(Ser307=)
+/. - c.921del r.(?) p.(Ser307ArgfsTer21)
+/. - c.922G>A r.(?) p.(Gly308Arg)
-/. - c.930G>C r.(?) p.(Val310=)
-?/. - c.930G>C r.(?) p.(Val310=)
-?/. - c.938C>T r.(?) p.(Pro313Leu)
?/. - c.1011G>A r.(?) p.(Ser337=)
-?/. - c.1030-12G>C r.(=) p.(=)
-?/. - c.1062C>A r.(?) p.(Asp354Glu)
+/. - c.1069C>T r.(?) p.(Arg357Ter)
+/. - c.1069C>T r.(?) p.(Arg357Ter)
-?/. - c.1079+8G>T r.(=) p.(=)
-?/. - c.1080G>A r.(?) p.(Arg360=)
?/. - c.1130A>G r.(?) p.(Lys377Arg)
-?/. - c.1158C>G r.(?) p.(Ser386Arg)
?/. - c.1165G>A r.(?) p.(Glu389Lys)
+/. - c.1173del r.(?) p.(Asp393Thrfs*29)
+/. - c.1173del r.(?) p.(Asp393Thrfs*29)
-?/. - c.1188G>A r.(?) p.(Gln396=)
-?/. - c.1188G>A r.(?) p.(Gln396=)
?/. - c.1204G>A r.(?) p.(Gly402Ser)
+/. - c.1275del r.(?) p.(Glu426ArgfsTer3)
-?/. - c.1312-6G>A r.(=) p.(=)
+/. - c.1312-1G>A r.(?) p.?
-?/. - c.1317G>A r.(?) p.(Gln439=)
-?/. - c.1317G>A r.(?) p.(Gln439=)
-?/. - c.1320G>A r.(?) p.(Gln440=)
+/. - c.1331G>A r.(?) p.(Trp444Ter)
-/. - c.1332G>A r.(?) p.(Trp444Ter)
-/. - c.1393G>A r.(?) p.(Glu465Lys)
-?/. - c.1393G>A r.(?) p.(Glu465Lys)
-/. - c.1393G>A r.(?) p.(Glu465Lys)
+/. - c.1426C>T r.(?) p.(Gln476Ter)
-/. - c.1506C>T r.(?) p.(Leu502=)
+/. - c.1525C>T r.(?) p.(Arg509Ter)
+/. - c.1525C>T r.(?) p.(Arg509Ter)
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