Transcript #00006524 (NM_207437.3, DNAH10 gene)

Transcript name dynein, axonemal, heavy chain 10
Gene name DNAH10 (dynein, axonemal, heavy chain 10)
Chromosome 12
Transcript - NCBI ID NM_207437.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_997320.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-4596del r.(?) p.(=)
-/. - c.-4596del r.(?) p.(=)
-/. - c.-4596dup r.(?) p.(=)
?/. - c.-4595A>T r.(?) p.(=)
-/. - c.-4595A>T r.(?) p.(=)
-?/. - c.-4595_-4592del r.(?) p.(=)
-?/. - c.-4594G>T r.(?) p.(=)
-?/. - c.-4593G>T r.(?) p.(=)
-?/. - c.-4592G>T r.(?) p.(=)
-?/. - c.-4591_-4590insTTTT r.(?) p.(=)
-?/. - c.-4510A>G r.(?) p.(=)
-?/. - c.40C>T r.(?) p.(Pro14Ser)
-?/. - c.270T>C r.(?) p.(Leu90=)
-?/. - c.474G>A r.(?) p.(Arg158=)
-/. - c.499T>C r.(?) p.(Ser167Pro)
-/. - c.659-16A>G r.(=) p.(=)
-/. - c.708T>C r.(?) p.(Ser236=)
-?/. - c.785C>T r.(?) p.(Ala262Val)
-?/. - c.786G>A r.(?) p.(Ala262=)
-?/. - c.817G>A r.(?) p.(Gly273Ser)
?/. - c.1103T>C r.(?) p.(Met368Thr)
-?/. - c.1103T>C r.(?) p.(Met368Thr)
?/. - c.1115G>A r.(?) p.(Arg372Gln)
?/. - c.1211G>A r.(?) p.(Arg404Gln)
-/. - c.1222C>T r.(?) p.(Leu408=)
-/. - c.1270T>C r.(?) p.(Leu424=)
?/. - c.1330A>T r.(?) p.(Ile444Leu)
-/. - c.1438A>G r.(?) p.(Ile480Val)
-?/. - c.1584C>T r.(?) p.(Ser528=)
?/. - c.1742G>A r.(?) p.(Arg581Gln)
-/. - c.1752T>C r.(?) p.(His584=)
?/. - c.1778A>G r.(?) p.(Gln593Arg)
-/. - c.1818A>G r.(?) p.(Gln606=)
?/. - c.2003C>T r.(?) p.(Pro668Leu)
-/. - c.2151G>T r.(?) p.(Met717Ile)
-?/. - c.2195A>G r.(?) p.(Asp732Gly)
-/. - c.2265C>T r.(?) p.(Ile755=)
-/. - c.2317G>A r.(?) p.(Val773Ile)
-?/. - c.2700G>C r.(?) p.(Leu900=)
-/. - c.2703G>A r.(?) p.(Thr901=)
?/. - c.2742C>T r.(?) p.(Ile914=)
-/. - c.2983C>T r.(?) p.(Arg995Trp)
-/. - c.2983C>T r.(?) p.(Arg995Trp)
?/. - c.3109C>T r.(?) p.(Arg1037Cys)
-/. - c.3110G>A r.(?) p.(Arg1037His)
-/. - c.3157C>T r.(?) p.(His1053Tyr)
?/. - c.3221A>G r.(?) p.(Asn1074Ser)
-/. - c.3299A>G r.(?) p.(Asn1100Ser)
-/. - c.3556G>A r.(?) p.(Glu1186Lys)
-/. - c.4405C>T r.(?) p.(Leu1469=)
-?/. - c.4503G>A r.(?) p.(Pro1501=)
-/. - c.4548+12G>A r.(=) p.(=)
-/. - c.4552A>G r.(?) p.(Met1518Val)
-/. - c.4557T>C r.(?) p.(Gly1519=)
-/. - c.4575C>A r.(?) p.(Pro1525=)
-/. - c.4627G>A r.(?) p.(Val1543Ile)
-/. - c.4671C>T r.(?) p.(Tyr1557=)
-/. - c.4891T>G r.(?) p.(Leu1631Val)
-?/. - c.5006+19A>G r.(=) p.(=)
-/. - c.5049C>T r.(?) p.(Ala1683=)
?/. - c.5099C>A r.(?) p.(Ala1700Glu)
-/. - c.5171C>T r.(?) p.(Thr1724Met)
-/. - c.5291G>A r.(?) p.(Arg1764Gln)
-/. - c.5301C>A r.(?) p.(Asp1767Glu)
?/. - c.5366C>T r.(?) p.(Thr1789Met)
-?/. - c.5382C>T r.(?) p.(Tyr1794=)
-?/. - c.5508C>T r.(?) p.(Thr1836=)
-/. - c.5594G>A r.(?) p.(Arg1865Lys)
-/. - c.5670T>C r.(?) p.(Asp1890=)
-?/. - c.5686G>A r.(?) p.(Val1896Met)
-/. - c.5686G>A r.(?) p.(Val1896Met)
-/. - c.5938-20T>C r.(=) p.(=)
-/. - c.5957C>T r.(?) p.(Thr1986Met)
-/. - c.5957C>T r.(?) p.(Thr1986Met)
-/. - c.5957C>T r.(?) p.(Thr1986Met)
?/. - c.5966A>G r.(?) p.(Tyr1989Cys)
?/. - c.6117G>C r.(?) p.(Met2039Ile)
?/. - c.6160G>A r.(?) p.(Gly2054Ser)
-?/. - c.6222C>T r.(?) p.(Asn2074=)
-?/. - c.6649G>C r.(?) p.(Glu2217Gln)
-?/. - c.6649G>C r.(?) p.(Glu2217Gln)
-/. - c.7004T>A r.(?) p.(Leu2335His)
-/. - c.7089C>T r.(?) p.(Asp2363=)
?/. - c.7102C>T r.(?) p.(Arg2368Cys)
-?/. - c.7121C>T r.(?) p.(Thr2374Ile)
-/. - c.7207C>T r.(?) p.(Arg2403Trp)
-/. - c.7448A>G r.(?) p.(Asn2483Ser)
-?/. - c.7467G>A r.(?) p.(Thr2489=)
-?/. - c.7527C>T r.(?) p.(Tyr2509=)
-/. - c.7547G>A r.(?) p.(Arg2516His)
-/. - c.7839C>T r.(?) p.(His2613=)
-/. - c.7844C>T r.(?) p.(Ser2615Leu)
?/. - c.8205G>C r.(?) p.(Gln2735His)
-/. - c.8281-10_8281-9del r.(=) p.(=)
-/. - c.8281-9del r.(=) p.(=)
?/. - c.8281-9dup r.(=) p.(=)
-?/. - c.8470-15G>T r.(=) p.(=)
-/. - c.8470-5C>T r.spl? p.?
-/. - c.8616G>A r.(?) p.(Glu2872=)
-/. - c.8676A>G r.(?) p.(Lys2892=)
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