Transcript #00024612 (NM_014615.3, GSE1 gene)

Transcript name transcript variant 1
Gene name GSE1 (Gse1 coiled-coil protein)
Chromosome 16
Transcript - NCBI ID NM_014615.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_055430.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2017-08-08 12:46:08 +02:00 (CEST)
Date last edited N/A


Variants

81 entries on 1 page. Showing entries 1 - 81.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-1859T>C r.(?) p.(=)
-?/. - c.16C>T r.(?) p.(His6Tyr)
?/. - c.35C>T r.(?) p.(Ser12Leu)
-?/. - c.70G>A r.(?) p.(Ala24Thr)
?/. - c.132C>T r.(?) p.(=)
?/. - c.142A>C r.(?) p.(Ser48Arg)
?/. - c.286C>G r.(?) p.(Pro96Ala)
?/. - c.304C>T r.(?) p.(Arg102Cys)
?/. - c.304C>T r.(?) p.(Arg102Cys)
?/. - c.319C>G r.(?) p.(Pro107Ala)
-?/. - c.348C>T r.(?) p.(Ser116=)
?/. - c.395T>C r.(?) p.(Val132Ala)
-?/. - c.423G>A r.(?) p.(Arg141=)
?/. - c.458G>A r.(?) p.(Arg153Gln)
?/. - c.509C>T r.(?) p.(Pro170Leu)
?/. - c.517C>G r.(?) p.(Pro173Ala)
-?/. - c.553C>G r.(?) p.(Leu185Val)
?/. - c.593C>T r.(?) p.(Pro198Leu)
?/. - c.608G>A r.(?) p.(Arg203Gln)
?/. - c.691C>T r.(?) p.(Leu231Phe)
?/. - c.713C>T r.(?) p.(Pro238Leu)
?/. - c.799A>T r.(?) p.(Met267Leu)
?/. - c.799A>T r.(?) p.(Met267Leu)
?/. - c.887C>T r.(?) p.(Ala296Val)
?/. - c.887C>T r.(?) p.(Ala296Val)
?/. - c.910G>A r.(?) p.(Val304Ile)
?/. - c.925G>A r.(?) p.(Glu309Lys)
-?/. - c.1028G>A r.(?) p.(Arg343His)
-?/. - c.1029C>T r.(?) p.(Arg343=)
?/. - c.1035_1070dup r.(?) p.(Arg347_Glu358dup)
?/. - c.1039C>T r.(?) p.(Arg347Cys)
-?/. - c.1039C>T r.(?) p.(Arg347Cys)
?/. - c.1040_1153del r.(?) p.(Arg347_Glu384del)
-?/. - c.1041_1046dup r.(?) p.(Arg351_Glu352dup)
-?/. - c.1051_1056dup r.(?) p.(Arg351_Glu352dup)
?/. - c.1052G>A r.(?) p.(Arg351His)
?/. - c.1052G>A r.(?) p.(Arg351His)
?/. - c.1117A>T r.(?) p.(Lys373Ter)
-?/. - c.1236C>T r.(?) p.(Ala412=)
-?/. - c.1313-5dup r.spl? p.?
?/. - c.1343C>T r.(?) p.(Pro448Leu)
?/. - c.1376C>T r.(?) p.(Pro459Leu)
-?/. - c.1555C>A r.(?) p.(Arg519=)
?/. - c.1604C>T r.(?) p.(Pro535Leu)
?/. - c.1756A>T r.(?) p.(Asn586Tyr)
?/. - c.1792C>T r.(?) p.(Arg598Trp)
?/. - c.1823A>T r.(?) p.(His608Leu)
-?/. - c.1863G>A r.(?) p.(Pro621=)
?/. - c.1889G>A r.(?) p.(Cys630Tyr)
-?/. - c.2014_2019dup r.(?) p.(Gly672_Pro673dup)
?/. - c.2063A>C r.(?) p.(Gln688Pro)
?/. - c.2110G>A r.(?) p.(Gly704Arg)
-?/. - c.2168C>T r.(?) p.(Ala723Val)
?/. - c.2182G>A r.(?) p.(Glu728Lys)
?/. - c.2204G>C r.(?) p.(Arg735Thr)
?/. - c.2216A>T r.(?) p.(Lys739Met)
-?/. - c.2274C>T r.(?) p.(Asp758=)
-?/. - c.2309A>T r.(?) p.(Glu770Val)
?/. - c.2353A>T r.(?) p.(Lys785Ter)
?/. - c.2447G>A r.(?) p.(Arg816Lys)
?/. - c.2507G>A r.(?) p.(Arg836Gln)
-?/. - c.2514G>A r.(?) p.(Thr838=)
-/. - c.2544C>T r.(?) p.(Arg848=)
?/. - c.2632G>A r.(?) p.(Glu878Lys)
?/. - c.2645-1G>C r.spl? p.?
?/. - c.2675C>G r.(?) p.(Ala892Gly)
?/. - c.2730G>T r.(?) p.(=)
?/. - c.2734G>C r.(?) p.(Asp912His)
-?/. - c.2882C>T r.(?) p.(Ser961Leu)
-?/. - c.2882C>T r.(?) p.(Ser961Leu)
?/. - c.3064G>C r.(?) p.(Glu1022Gln)
-?/. - c.3130+9G>A r.(=) p.(=)
-?/. - c.3131-3C>T r.spl? p.?
-?/. - c.3181G>A r.(?) p.(Val1061Ile)
?/. - c.3207G>T r.(?) p.(Gln1069His)
-?/. - c.3218G>A r.(?) p.(Arg1073His)
?/. - c.3312_3314del r.(?) p.(Glu1107del)
-?/. - c.3327T>A r.(?) p.(Asp1109Glu)
?/. - c.3469C>T r.(?) p.(Arg1157Trp)
?/. - c.3563G>A r.(?) p.(Arg1188Gln)
-?/. - c.*5991C>T r.(=) p.(=)
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