Transcript #00018398 (NM_015474.3, SAMHD1 gene)

Transcript name SAM domain and HD domain 1
Gene name SAMHD1 (SAM domain and HD domain 1)
Chromosome 20
Transcript - NCBI ID NM_015474.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_056289.2
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

100 entries on 1 page. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/+? _1_1i c.-6085_208+2691del r.0? p.0?
+?/+? _1_1i c.-6085_208+2691del r.0? p.0?
+?/+? _1_1i c.-6085_208+2691del r.0? p.0?
+?/+? _1_1i c.-6085_208+2691del r.0? p.0?
+?/+? _1_1i c.-6085_208+2691del r.0? p.0?
+?/+? _1_1i c.-6085_208+2691del r.0? p.0?
+?/+? _1_1i c.-6085_208+2691del r.0? p.0?
+?/+? _1_1i c.-6085_208+2691del r.0? p.0?
+?/+? _1_1i c.-6085_208+2691del r.0? p.0?
+?/+? _1_1i c.-6085_208+2691del r.0? p.0?
+/+? _1_13i c.(?_-1)_(1503+1_1504-1)del r.0 p.0
-?/. - c.77C>T r.(?) p.(Pro26Leu)
-?/. - c.102G>A r.(?) p.(Pro34=)
-?/. - c.114C>G r.(?) p.(Leu38=)
-?/. - c.237T>C r.(?) p.(Pro79=)
-?/. - c.237T>C r.(?) p.(Pro79=)
-?/. - c.275+8T>A r.(=) p.(=)
-?/. - c.334G>A r.(?) p.(Val112Ile)
-?/. - c.348+18T>G r.(=) p.(=)
+/. 4 c.359_370del r.(?) p.(Asp120_His123del)
+/. 4 c.368A>C r.(?) p.(His123Pro)
?/? 4 c.400C>T r.(?) p.(Arg134*)
+/. - c.400C>T r.(?) p.(Arg134*)
+/. 4 c.427C>T r.(?) p.(Arg143Cys)
+/. 4 c.428G>A r.(?) p.(Arg143His)
?/. - c.428G>A r.(?) p.(Arg143His)
+/. 4 c.433C>T r.(?) p.(Arg145*)
+/. - c.433C>T r.(?) p.(Arg145*)
+/. 4 c.434G>A r.(?) p.(Arg145Gln)
?/. - c.434G>C r.(?) p.(Arg145Pro)
+/+ 4 c.445C>T r.(?) p.(Gln149*)
-?/. - c.462C>T r.(?) p.(Tyr154=)
+/. 4 c.490C>T r.(?) p.(Arg164*)
+/. - c.490C>T r.(?) p.(Arg164Ter)
+/. 4 c.499C>T r.(?) p.(His167Tyr)
?/. - c.508G>A r.(?) p.(Gly170Arg)
-/. - c.510-190T>C r.(=) p.(=)
+/. 5 c.602T>A r.(?) p.(Ile201Asn)
+/. 5 c.602T>A r.(?) p.(Ile201Asn)
+/. 5 c.602T>A r.(?) p.(Ile201Asn)
+/. 5 c.602T>A r.(?) p.(Ile201Asn)
+/. 5 c.625G>A r.(?) p.(Gly209Ser)
+?/. - c.625+1G>A r.spl? p.?
-/. - c.625+43C>A r.(=) p.(=)
-?/. - c.626-5T>C r.spl? p.?
-?/. - c.626-5T>C r.spl? p.?
+/. - c.626-1G>A r.spl? p.?
+/. 5i c.626-1G>C r.[626_627ins[627-18_627-2;c],627_697del] p.[His210Serfs*5,Glu209Alafs*2]
+/. - c.646_647del r.(?) p.(Met216Valfs*2)
+/. - c.646_647del r.(?) p.(Met216Valfs*2)
+?/+? 6 c.648dup r.(?) p.(Phe217Valfs*2)
+?/+? 6 c.648dup r.(?) p.(Phe217Valfs*2)
+?/+? 6 c.648dup r.(?) p.(Phe217Valfs*2)
?/. - c.676C>T r.(?) p.(Arg226Cys)
-?/. - c.681G>A r.(?) p.(Pro227=)
-?/. - c.697-11A>G r.(=) p.(=)
?/. - c.712G>A r.(?) p.(Val238Ile)
+/. 7 c.760A>G r.(?) p.(Met254Val)
+/. 7 c.869G>A r.(?) p.(Arg290His)
?/. - c.901G>C r.(?) p.(Val301Leu)
+?/. - c.901G>C r.(?) p.(Val301Leu)
?/. - c.901G>C r.(?) p.(Val301Leu)
?/. - c.933C>A r.(?) p.(Asp311Glu)
-?/. - c.954-4C>G r.spl? p.?
?/. - c.998G>A r.(?) p.(Arg333His)
?/. - c.1019T>A r.(?) p.(Val340Asp)
?/. - c.1096C>T r.(?) p.(Arg366Cys)
+/. 10 c.1098dup r.(?) p.(Asn367Glnfs*6)
+?/+? 10 c.1106T>C r.(?) p.(Leu369Ser)
+/. 10 c.1153A>G r.(?) p.(Met385Val)
-?/. - c.1154+15T>G r.(=) p.(=)
-?/. - c.1154+135A>T r.(=) p.(=)
?/. - c.1223G>C r.(?) p.(Arg408Pro)
+?/+? 11i_16i c.1273_*2del r.(?) p.(Asn425ValfsTer48)
-?/. - c.1320C>T r.(?) p.(Asp440=)
-?/. - c.1340A>C r.(?) p.(Gln447Pro)
+/. 12 c.1343T>C r.(?) p.(Ile448Thr)
?/. - c.1393C>A r.(?) p.(Gln465Lys)
+?/+? 12i c.1411-2A>G r.spl? p.(=)
+?/+? 12i c.1411-2A>G r.spl? p.(=)
+?/+? 12i c.1411-2A>G r.spl? p.(=)
+?/+? 12i c.1411-2A>G r.spl? p.(=)
-?/. - c.1445G>A r.(?) p.(Ser482Asn)
-?/. - c.1470C>T r.(?) p.(Asp490=)
+?/+? 13 c.1476del r.(?) p.(Lys492Asnfs*2)
+?/+? 13 c.1476del r.(?) p.(Lys492Asnfs*2)
-?/. - c.1482G>A r.(?) p.(Lys494=)
+?/+? 13i c.1503+1G>T r.spl? p.(=)
?/. - c.1593G>C r.(?) p.(Arg531Ser)
-?/. - c.1609-4A>C r.spl? p.?
+/. 14i c.1609-1G>C r.spl? p.(=)
+/. - c.1618del r.(?) p.(Leu540Phefs*10)
+/. 15 c.1642C>T r.(?) p.(Gln548*)
+?/. - c.1651C>G r.(?) p.(Arg551Gly)
+/. - c.1651C>T r.(?) p.(Arg551Ter)
-?/. 15 c.1657T>C r.(?) p.(Tyr553His)
-?/. - c.1743G>A r.(?) p.(Pro581=)
+?/+? 15i c.1746+1G>T r.spl? p.(=)
?/. - c.1747-1G>T r.spl? p.?
?/. - c.1756G>T r.(?) p.(Val586Phe)
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