Transcript #00006528 (NM_173628.3, DNAH17 gene)

Transcript name dynein, axonemal, heavy chain 17
Gene name DNAH17 (dynein, axonemal, heavy chain 17)
Chromosome 17
Transcript - NCBI ID NM_173628.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_775899.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-26+7G>A r.(=) p.(=)
-?/. - c.18C>T r.(?) p.(Asp6=)
-?/. - c.144C>A r.(?) p.(Asp48Glu)
-?/. - c.332C>A r.(?) p.(Ala111Glu)
-?/. - c.393C>G r.(?) p.(Pro131=)
-/. - c.441T>C r.(?) p.(Asn147=)
-?/. - c.594C>T r.(?) p.(=)
-?/. - c.663C>T r.(?) p.(His221=)
-?/. - c.833-7C>T r.(=) p.(=)
-?/. - c.1157C>T r.(?) p.(Thr386Met)
?/. - c.1267C>T r.(?) p.(Arg423Cys)
+?/. 10 c.1293_1294del r.(?) p.(Tyr431*)
-?/. - c.1864A>G r.(?) p.(Thr622Ala)
-/. - c.1871A>G r.(?) p.(Gln624Arg)
-?/. - c.2287+4C>T r.spl? p.?
?/. - c.2830C>T r.(?) p.(Arg944Trp)
?/. - c.2830C>T r.(?) p.(Arg944Trp)
?/. - c.2830C>T r.(?) p.(Arg944Trp)
-/. - c.3114+5G>A r.spl? p.?
-?/. - c.3114+7G>A r.(=) p.(=)
?/. - c.3122C>A r.(?) p.(Ser1041Tyr)
-?/. - c.3508-5C>T r.spl? p.?
-?/. - c.3516G>A r.(?) p.(Pro1172=)
-?/. - c.3660C>G r.(?) p.(Arg1220=)
-?/. - c.3661G>A r.(?) p.(Glu1221Lys)
-?/. - c.3730G>A r.(?) p.(Ala1244Thr)
?/. - c.3821G>A r.(?) p.(Arg1274Gln)
-?/. - c.4035G>A r.(?) p.(Thr1345=)
?/. - c.4042C>T r.(?) p.(Arg1348Cys)
?/. - c.4042C>T r.(?) p.(Arg1348Cys)
?/. - c.4541C>T r.(?) p.(Pro1514Leu)
?/. - c.4788C>T r.(?) p.(=)
?/. - c.4798G>A r.(?) p.(Val1600Met)
?/. - c.4798G>T r.(?) p.(Val1600Leu)
+?/. 36 c.5486G>A r.(?) p.(Cys1829Tyr)
-?/. - c.5922C>T r.(?) p.(Val1974=)
?/. - c.6250C>T r.(?) p.(Arg2084Trp)
?/. - c.6263T>G r.(?) p.(Phe2088Cys)
-?/. - c.6379G>A r.(?) p.(Val2127Ile)
-?/. - c.6390G>A r.(?) p.(=)
?/. - c.6407A>C r.(?) p.(Gln2136Pro)
-?/. - c.6420C>A r.(?) p.(Ser2140=)
-?/. - c.6462C>T r.(?) p.(Ala2154=)
?/. - c.6639G>C r.(?) p.(Glu2213Asp)
-?/. - c.6669+4C>T r.spl? p.?
?/. - c.6669+5G>A r.spl? p.?
-?/. - c.6669+7G>A r.(=) p.(=)
?/. - c.6880C>A r.(?) p.(Leu2294Ile)
?/. - c.7261G>A r.(?) p.(Asp2421Asn)
?/. - c.7483+5G>A r.spl? p.?
-?/. - c.7650-5C>T r.spl? p.?
-?/. - c.7698C>T r.(?) p.(Tyr2566=)
?/. - c.7780T>A r.(?) p.(Phe2594Ile)
-?/. - c.7827G>A r.(?) p.(Thr2609=)
-?/. - c.7901C>T r.(?) p.(Ala2634Val)
+/. 52 c.7994_8012del r.(?) p.(Gly2665Glufs*4)
?/. - c.8089G>A r.(?) p.(Val2697Ile)
-?/. - c.8132C>T r.(?) p.(Ala2711Val)
?/. - c.8186C>T r.(?) p.(Pro2729Leu)
-?/. - c.8244C>T r.(?) p.(Thr2748=)
-?/. - c.8512-6G>A r.(=) p.(=)
?/. - c.8570T>C r.(?) p.(Leu2857Pro)
?/. - c.9049C>A r.(?) p.(Pro3017Thr)
?/. - c.9104G>C r.(?) p.(Arg3035Thr)
-?/. - c.9237C>T r.(?) p.(Ser3079=)
-?/. - c.9261C>T r.(?) p.(Val3087=)
?/. - c.9322G>A r.(?) p.(Val3108Ile)
?/. - c.9815T>A r.(?) p.(Leu3272Gln)
-?/. - c.9978-10C>A r.(=) p.(=)
?/. - c.10096G>A r.(?) p.(Val3366Met)
?/. - c.10258C>T r.(?) p.(Pro3420Ser)
-?/. - c.10305C>T r.(?) p.(=)
-?/. - c.10323C>T r.(?) p.(Ile3441=)
+/. 65 c.10486_10497dup r.(?) p.(Val3496_Pro3499dup)
?/. - c.10496C>T r.(?) p.(Pro3499Leu)
+?/. 65 c.10496C>T r.(?) p.(Pro3499Leu)
?/. - c.10514C>T r.(?) p.(Thr3505Met)
?/. - c.10529+8_10529+10del r.(=) p.(=)
-?/. - c.10529+8_10529+10del r.(=) p.(=)
?/. - c.10572G>T r.(?) p.(Lys3524Asn)
+?/. - c.10784T>C r.(?) p.(Leu3595Pro)
+/. 67 c.10784T>C r.(?) p.(Leu3595Pro)
?/. - c.10805G>T r.(?) p.(Arg3602Leu)
-?/. - c.10821G>A r.(?) p.(Ser3607=)
?/. - c.10900G>A r.(?) p.(Val3634Met)
-?/. - c.10941G>A r.(?) p.(Ala3647=)
-?/. - c.10965G>A r.(?) p.(Ala3655=)
?/. - c.11159G>A r.(?) p.(Arg3720Gln)
?/. - c.11204C>T r.(?) p.(Thr3735Met)
-?/. - c.11212-7C>T r.(=) p.(=)
-?/. - c.11391C>T r.(?) p.(Ala3797=)
-?/. - c.11679A>G r.(?) p.(Gly3893=)
-?/. - c.11679A>G r.(?) p.(Gly3893=)
?/. - c.11761G>T r.(?) p.(Ala3921Ser)
-?/. - c.11806-5T>C r.spl? p.?
?/. - c.11824C>T r.(?) p.(Arg3942Trp)
?/. - c.11987C>T r.(?) p.(Thr3996Met)
-?/. - c.12018G>A r.(?) p.(Leu4006=)
?/. - c.12121C>T r.(?) p.(Arg4041Cys)
-?/. - c.12192C>T r.(?) p.(Asn4064=)
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