Transcript #00006519 (NM_001369.2, DNAH5 gene)

Transcript name dynein, axonemal, heavy chain 5
Gene name DNAH5 (dynein, axonemal, heavy chain 5)
Chromosome 5
Transcript - NCBI ID NM_001369.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001360.1
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

413 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-1992899_*2718680del r.0? p.0?
?/. _1_47i c.(?_-42)_(7887+1_7888-1)dup r.? p.?
-?/. - c.11T>C r.(?) p.(Ile4Thr)
-/. - c.36T>G r.(?) p.(His12Gln)
-/. - c.36T>G r.(?) p.(His12Gln)
-/. - c.58-13T>C r.(=) p.(=)
-/. - c.71G>A r.(?) p.(Gly24Glu)
-/. - c.71G>A r.(?) p.(Gly24Glu)
?/. - c.88C>T r.(?) p.(Arg30Trp)
?/. - c.116A>G r.(?) p.(Tyr39Cys)
-/. - c.192+14C>G r.(=) p.(=)
-/. - c.192+14C>G r.(=) p.(=)
?/. - c.278-3T>C r.(?) p.(=)
+?/. - c.356del r.(?) p.(Asn119Thrfs*30)
+?/. - c.382G>A r.(?) p.(Val128Met)
-?/. - c.574G>A r.(?) p.(Ala192Thr)
-?/. - c.624C>T r.(?) p.(Asn208=)
?/. - c.633G>A r.(?) p.(Ser211=)
?/. - c.676T>C r.(?) p.(Cys226Arg)
-?/. - c.727C>G r.(?) p.(Leu243Val)
?/. - c.793G>A r.(?) p.(Glu265Lys)
-?/. - c.894C>G r.(?) p.(Asn298Lys)
-?/. - c.971T>C r.(?) p.(Leu324Pro)
-?/. - c.975+4G>A r.spl? p.?
?/. - c.981G>T r.(?) p.(Trp327Cys)
+/. - c.1089+1G>A r.spl? p.?
+/. - c.1089+1G>A r.spl? p.?
?/. - c.1121T>C r.(?) p.(Ile374Thr)
?/. - c.1121T>C r.(?) p.(Ile374Thr)
?/. - c.1121T>C r.(?) p.(Ile374Thr)
?/. - c.1198G>A r.(?) p.(Val400Met)
?/. - c.1206T>A r.(?) p.(Asn402Lys)
-?/. - c.1206T>A r.(?) p.(Asn402Lys)
?/. - c.1206T>A r.(?) p.(Asn402Lys)
-?/. - c.1206T>A r.(?) p.(Asn402Lys)
-?/. - c.1252G>A r.(?) p.(Ala418Thr)
-?/. - c.1329G>A r.(?) p.(Gln443=)
-?/. - c.1335C>T r.(?) p.(=)
?/. - c.1433G>A r.(?) p.(Arg478Gln)
?/. - c.1435C>T r.(?) p.(Arg479Cys)
?/. - c.1502T>C r.(?) p.(Ile501Thr)
-/. - c.1503T>C r.(?) p.(Ile501=)
-/. - c.1503T>C r.(?) p.(Ile501=)
-?/. - c.1631C>T r.(?) p.(Thr544Ile)
-?/. - c.1647C>G r.(?) p.(Asn549Lys)
-?/. - c.1658A>G r.(?) p.(Lys553Arg)
?/. - c.1667A>G r.(?) p.(Asp556Gly)
?/. - c.1667A>G r.(?) p.(Asp556Gly)
-/. - c.1672A>G r.(?) p.(Thr558Ala)
-/. - c.1672A>G r.(?) p.(Thr558Ala)
?/. - c.1710A>T r.(?) p.(Arg570Ser)
?/. - c.1715T>G r.(?) p.(Leu572Trp)
+/. - c.1730+2T>C r.spl? p.?
-/. - c.1772T>G r.(?) p.(Leu591Arg)
?/. - c.1810T>C r.(?) p.(Ser604Pro)
?/. - c.1858C>A r.(?) p.(Gln620Lys)
-/. - c.2053-23A>C r.spl? p.?
-/. - c.2229T>C r.(?) p.(Asp743=)
-/. - c.2229T>C r.(?) p.(Asp743=)
-?/. - c.2253C>A r.(?) p.(Asn751Lys)
-/. - c.2253C>A r.(?) p.(Asn751Lys)
?/? ? c.2253C>A r.(?) p.(Asn751Lys)
-?/. - c.2253C>A r.(?) p.(Asn751Lys)
?/. - c.2259+3A>G r.spl? p.?
-/. - c.2296A>T r.(?) p.(Ile766Leu)
-/. - c.2296A>T r.(?) p.(Ile766Leu)
-?/. - c.2368G>A r.(?) p.(Ala790Thr)
-?/. - c.2400G>A r.(?) p.(Glu800=)
-?/. - c.2432-2del r.spl? p.?
?/. - c.2443T>A r.(?) p.(Leu815Met)
-?/. - c.2461A>G r.(?) p.(Asn821Asp)
-?/. - c.2577+5T>A r.spl? p.?
-?/. - c.2578-10_2578-7del r.(=) p.(=)
-?/. - c.2578-9_2578-7del r.(=) p.(=)
-?/. - c.2578-9_2578-7del r.(=) p.(=)
-?/. - c.2578-9_2578-7del r.(=) p.(=)
-/. - c.2578-8_2578-7del r.(=) p.(=)
-?/. - c.2578-8_2578-7del r.(=) p.(=)
-?/. - c.2578-8_2578-6del r.(=) p.(=)
-/. - c.2578-7del r.(=) p.(=)
-?/. - c.2578-7del r.(=) p.(=)
-/. - c.2578-7del r.(=) p.(=)
-?/. - c.2578-7_2578-6del r.(=) p.(=)
-?/. - c.2578-6G>T r.(=) p.(=)
-?/. - c.2578-5G>T r.spl? p.?
-?/. - c.2578-2A>T r.spl? p.?
-?/. - c.2578-2_2578-1del r.spl? p.?
-?/. - c.2581C>T r.(?) p.(Leu861Phe)
-?/. - c.2585G>T r.(?) p.(Cys862Phe)
-?/. - c.2587G>T r.(?) p.(Val863Leu)
-?/. - c.2593G>T r.(?) p.(Gly865Cys)
?/. - c.2597C>T r.(?) p.(Ala866Val)
-/. - c.2683G>A r.(?) p.(Glu895Lys)
-?/. - c.2821G>A r.(?) p.(Val941Ile)
-/. - c.2868C>A r.(=) p.(=)
?/. - c.2869G>A r.(?) p.(Glu957Lys)
-?/. - c.3013A>T r.(?) p.(Asn1005Tyr)
-?/. - c.3112G>A r.(?) p.(Val1038Met)
-?/. - c.3175-3T>C r.spl? p.?
-/. - c.3241A>G r.(?) p.(Met1081Val)
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