Transcript #00025313 (NM_001101802.1, PHF21A gene)

Transcript name transcript variant 1
Gene name PHF21A (PHD finger protein 21A)
Chromosome 11
Transcript - NCBI ID NM_001101802.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001095272.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2018-08-13 08:41:44 +02:00 (CEST)
Date last edited N/A


Variants

78 entries on 1 page. Showing entries 1 - 78.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.(-1_*1)::[NM_013427.2:(-1_*1)] r.? p.?
+/. 14i c.1449+2321::[NM_001419.2:657-1442] r.? p.?
+/. 5i c.153+34607::? r.? p.?
+/. 5i c.?::insATTTGGAG;153+34610 r.? p.?
+/. 14i c.[NM_001419.2:657-1435]::1449+2321 r.? p.?
+/. _1_18_ c.0 r.0 p.0
+/. _1_18_ c.0 r.0 p.0
+/. _1_18_ c.0 r.0 p.0
+/. _1_18_ c.0 r.0 p.0
+/. _1_18_ c.0 r.0 p.0
-?/. - c.154-5G>T r.spl? p.?
?/. - c.206C>T r.(?) p.(Pro69Leu)
+/. - c.270dup r.(?) p.(Pro91Thrfs*82)
?/. - c.314A>G r.(?) p.(His105Arg)
?/. - c.361-1del r.spl? p.?
?/. - c.424A>G r.(?) p.(Thr142Ala)
+?/. - c.599del r.(?) p.(Asn200Thrfs*67)
+?/. - c.657_658insAA r.(?) p.(Pro220Asnfs*48)
+?/. - c.956_959del r.(?) p.(Gln319LeufsTer53)
+?/. - c.961del r.(?) p.(Val321TyrfsTer52)
+?/. - c.965dup r.(?) p.(Leu323AlafsTer2)
-?/. - c.967C>T r.(?) p.(Leu323Phe)
?/. - c.993+2T>C r.spl? p.?
+?/. 11 c.1034_1037del r.(?) p.(Glu345Alafs*27)
?/. - c.1042A>G r.(?) p.(Thr348Ala)
?/. - c.1042A>G r.(?) p.(Thr348Ala)
?/. - c.1045A>G r.(?) p.(Ile349Val)
-?/. - c.1093-5C>T r.spl? p.?
?/. - c.1144+1G>A r.spl? p.?
+?/. - c.1144+2T>G r.spl? p.?
+/. - c.1168C>T r.(?) p.(Arg390*)
+?/. - c.1220dup r.(?) p.(Glu408Argfs*3)
?/. - c.1289G>A r.(?) p.(Arg430His)
-?/. - c.1295C>T r.(?) p.(Pro432Leu)
-?/. - c.1408C>T r.(?) p.(Pro470Ser)
?/. - c.1437C>A r.(?) p.(=)
+/. - c.1553dup r.(?) p.(Leu519Serfs*53)
+/. - c.1553dup r.(?) p.(Leu519Serfs*53)
-?/. - c.1666A>G r.(?) p.(Ile556Val)
+/. - c.1676_1681+15del r.spl? p.?
-?/. - c.1681+7A>C r.(=) p.(=)
-/. - c.1682-7_1682-3del r.spl? p.?
-/. - c.1682-6_1682-3del r.spl? p.?
-?/. - c.1682-5_1682-3del r.spl? p.?
-?/. - c.1682-4_1682-3del r.spl? p.?
-?/. - c.1682-4_1682-3del r.spl? p.?
-?/. - c.1682-3del r.spl? p.?
?/. - c.1682-3_1682-2del r.spl? p.?
+?/. - c.1738C>T r.(?) p.(Arg580Ter)
+/. - c.1738C>T r.(?) p.(Arg580Ter)
+?/. - c.1738C>T r.(?) p.(Arg580Ter)
+?/. - c.1738C>T r.(?) p.(Arg580*)
?/. - c.1785+470C>T r.(=) p.(=)
?/. - c.1810A>G r.(?) p.(Ile604Val)
-?/. - c.1810A>G r.(?) p.(Ile604Val)
-?/. - c.1851G>A r.(?) p.(Lys617=)
-?/. - c.1885G>A r.(?) p.(Asp629Asn)
-?/. - c.1949C>T r.(?) p.(Thr650Ile)
+?/. - c.1955del r.(?) p.(Pro652Leufs*104)
+/. - c.1956del r.(?) p.(Ala653Profs*103)
+/. - c.1956del r.(?) p.(Ala653ProfsTer103)
?/. - c.1956del r.(?) p.(Ala653ProfsTer103)
+/. - c.1956del r.(?) p.(Ala653ProfsTer103)
-?/. - c.1966G>A r.(?) p.(Ala656Thr)
-?/. - c.*5259C>T r.(=) p.(=)
?/. - c.*5265C>T r.(=) p.(=)
-?/. - c.*5774C>T r.(=) p.(=)
?/. - c.*7140G>A r.(=) p.(=)
?/. - c.*7146dup r.(?) p.(=)
?/. - c.*7154del r.(?) p.(=)
-?/. - c.*7466G>A r.(=) p.(=)
?/. - c.*7470_*7472del r.(=) p.(=)
?/. - c.*7746C>G r.(=) p.(=)
?/. - c.*7834T>C r.(=) p.(=)
-?/. - c.*9170G>A r.(=) p.(=)
?/. - c.*9180G>A r.(=) p.(=)
-?/. - c.*9368C>T r.(=) p.(=)
?/. - c.*9440T>C r.(=) p.(=)
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