Transcript #00000047 (NM_000527.4, LDLR gene)

Transcript name transcript variant 1
Gene name LDLR (low density lipoprotein receptor)
Chromosome 19
Transcript - NCBI ID NM_000527.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_000518.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

95 entries on 1 page. Showing entries 1 - 95.
Legend   How to query  

Affects function     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
+/. - c.-152C>T - r.(=) p.(=) - -
+/. 2 c.77_78del - r.(?) p.(Arg26Metfs*25) - ClinVar
-/. 2 c.81C>T - r.(=) p.(=) - ClinVar
+/. 2 c.81C>T p.Cys27Cys r.(=) p.(=) - Benign
./. 2i c.190+4A>T - r.spl? p.? - ClinVar
./. 2i c.190+56G>A - r.(=) p.(=) - ClinVar
+/. 2i c.190+58C>T - r.(=) p.(=) - -
+/. 2i c.190+58C>T - r.(=) p.(=) - -
+/. 3 c.268G>A - r.(?) p.(Asp90Asn) - ClinVar
+/. 3 c.268G>A - r.(?) p.(Asp90Asn) - ClinVar
-?/. 3 c.300C>T - r.(=) p.(=) - ClinVar
./. 3 c.301G>A - r.(?) p.(Glu101Lys) - ClinVar
./. 3 c.301G>A - r.(?) p.(Glu101Lys) - ClinVar
+/. 3 c.301G>A - r.(?) p.(Glu101Lys) - Pathogenic/Likely pathogenic
+/. 3i c.313+1G>A - r.spl? p.? - -
+/. 3i c.313+1G>A - r.spl? p.? - -
+/. 4 c.344G>A - r.(?) p.(Arg115His) - ClinVar
+?/. 4 c.415G>C - r.(?) p.(Asp139His) - ClinVar
+/. 4 c.415G>C - r.(?) p.(Asp139His) - Likely pathogenic
+/. 4 c.530C>T - r.(?) p.(Ser177Leu) - Pathogenic/Likely pathogenic
+?/. 4 c.601G>A - r.(?) p.(Glu201Lys) - ClinVar
+/. 4 c.601G>A - r.(?) p.(Glu201Lys) - Likely pathogenic​
+/. 4 c.660delC - r.(?) p.(Asp221Thrfs*44) - -
+/. 5 c.757C>T - r.(?) p.(Arg253Trp) - -
+/. 5 c.757C>T - r.(?) p.(Arg253Trp) - -
+?/. 5 c.763T>A - r.(?) p.(Cys255Ser) - ClinVar
+?/. 5 c.763T>A - r.(?) p.(Cys255Ser) - ClinVar
+?/. 5 c.763T>A - r.(?) p.(Cys255Ser) - ClinVar
+/. 5 c.763T>A - r.(?) p.(Cys255Ser) - ClinVar
+/. 5 c.763T>A - r.(?) p.(Cys255Ser) - ClinVar
+/. 5 c.763T>A - r.(?) p.(Cys255Ser) - Likely pathogenic​
+/. 6 c.829G>A - r.(?) p.(Glu277Lys) - -
./. 6 c.910G>A - r.(?) p.(Asp304Asn) - ClinVar
./. 6 c.910G>A - r.(?) p.(Asp304Asn) - ClinVar
+/. 6 c.910G>A - r.(?) p.(Asp304Asn) - Pathogenic/Likely pathogenic
-/. 6i c.940+36G>A - r.(=) p.(=) - ClinVar
+/. 6i c.940+36G>A - r.(=) p.(=) - Benign
+/. 6i c.940+775G>A - r.(=) p.(=) - -
+?/. 6i c.940+1187G>T - r.(=) p.(=) - -
+/. 7 c.986G>A - r.(?) p.(Cys329Tyr) - ClinVar
+/. 7i c.1060+7C>A - r.(=) p.(=) - -
+/. 7i c.1060+7C>T c.1060+7T>C r.(=) p.(=) - Uncertain significance
+/. 7i c.1060+10G>C - r.(=) p.(=) - -
+/. 8 c.1132C>T - r.(?) p.(Gln378*) - ClinVar
+/. 8 c.1132C>T - r.(?) p.(Gln378*) - ClinVar
-?/. 8i c.1186+41T>A - r.(=) p.(=) - ClinVar
./. 9 c.1194C>T - r.(=) p.(=) - ClinVar
+/. 9 c.1194C>T p.Ile398Ile r.(=) p.(=) - Conflicting interpretations of pathogenicity
+/. 9 c.1216C>T - r.(?) p.(Arg406Trp) - -
+/. 9 c.1216C>T - r.(?) p.(Arg406Trp) - -
+/. 9 c.1241T>G - r.(?) p.(Leu414Arg) - ClinVar
+/. 9 c.1241T>G - r.(?) p.(Leu414Arg) - ClinVar
+/. 9 c.1268T>C - r.(?) p.(Ile423Thr) - ClinVar
./. 9 c.1284C>G - r.(?) p.(Asn428Lys) - ClinVar
-/. 9i c.1359-30C>T - r.(=) p.(=) - ClinVar
-?/. 10 c.1411A>G - r.(?) p.(Arg471Gly) - ClinVar
-/. 10 c.1413A>G - r.(=) p.(=) - ClinVar
-/. 10 c.1413A>G - r.(=) p.(=) - ClinVar
+/. 10 c.1432G>A - r.(?) p.(Gly478Arg) - -
+/. 10 c.1474G>A - r.(?) p.(Asp492Asn) - -
./. 10i c.1586+5G>C - r.spl? p.? - ClinVar
-/. 11 c.1617C>T - r.(=) p.(=) - ClinVar
-/. 11 c.1617C>T - r.(=) p.(=) - ClinVar
+/. 11 c.1617C>T p.Pro539Pro r.(=) p.(=) - Benign
./. 11i c.1705+56C>T - r.(=) p.(=) - ClinVar
+/. 11i c.1705+56C>T - r.(=) p.(=) - Likely benign
-?/. 11i c.1705+112C>G - r.(=) p.(=) - ClinVar
+/. 11i c.1705+112C>G - r.(=) p.(=) - Likely benign
+/. 11i c.1705+117T>G - r.(=) p.(=) - -
+/. 11i c.1705+117T>G - r.(=) p.(=) - -
-/. 11i c.1706-69G>T - r.(=) p.(=) - ClinVar
-/. 11i c.1706-55A>C - r.(=) p.(=) - ClinVar
+/. 12 c.1706_1845dup - r.(?) p.(Asp616Ilefs*96) - -
./. 12 c.1729T>C - r.(?) p.(Trp577Arg) - ClinVar
./. 12 c.1773C>T - r.(=) p.(=) - ClinVar
./. 12 c.1773C>T - r.(=) p.(=) - ClinVar
./. 12 c.1773C>T - r.(=) p.(=) - ClinVar
+/. 12i c.1773C>T p.Asn591Asn r.(=) p.(=) - Benign/Likely benign​
./. 13 c.1959T>C - r.(=) p.(=) - ClinVar
./. 13 c.1959T>C - r.(=) p.(=) - ClinVar
+/. 14 c.1996_2012del - r.(?) p.(Trp666Profs*45) - ClinVar
+/. 14 c.2050G>A - r.(?) p.(Ala684Thr) - ClinVar
+/. 14 c.2087G>A - r.(?) p.(Cys696Tyr) - ClinVar
./. 14 c.2100C>G - r.(?) p.(Asp700Glu) - ClinVar
+/. 14 c.2108_2114dup - r.(?) p.(Arg706Alafs*13) - ClinVar
+?/. 14 c.2132G>A - r.(?) p.(Cys711Tyr) - ClinVar
+?/. 14 c.2132G>A - r.(?) p.(Cys711Tyr) - ClinVar
+?/. 14 c.2132G>A - r.(?) p.(Cys711Tyr) - Likely pathogenic
+/. 14 c.2132G>A - r.(?) p.(Cys711Tyr) - Likely pathogenic
-?/. 15 c.2209A>G - r.(?) p.(Arg737Gly) - ClinVar
-/. 15 c.2232A>G - r.(=) p.(=) - ClinVar
+/. 15 c.2232A>G p.Arg744Arg r.(=) p.(=) - Benign​
+/. 15i c.2311+1G>T - r.spl? p.? - -
+?/. 15i c.2312-1679T>C - r.(=) p.(=) - -
+/. 16 c.2389G>A - r.(?) p.(Val797Met) - -
Legend   How to query