Transcript #00014079 (NM_024690.2, MUC16 gene)

Transcript name mucin 16, cell surface associated
Gene name MUC16 (mucin 16, cell surface associated)
Chromosome 19
Transcript - NCBI ID NM_024690.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_078966.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.41C>T r.(?) p.(Thr14Ile)
-?/. - c.1020C>T r.(?) p.(Ala340=)
-?/. - c.1746T>A r.(?) p.(Leu582=)
-?/. - c.2254A>G r.(?) p.(Ile752Val)
?/. - c.2434T>C r.(?) p.(Ser812Pro)
?/. - c.2492C>T r.(?) p.(Ser831Leu)
-?/. - c.3056C>T r.(?) p.(Thr1019Ile)
?/. - c.3362C>T r.(?) p.(Pro1121Leu)
-?/. - c.3368A>G r.(?) p.(Asp1123Gly)
?/. 1 c.3445A>C r.(?) p.(Thr1149Pro)
-?/. - c.3828C>T r.(?) p.(Gly1276=)
?/. - c.4186T>G r.(?) p.(Leu1396Val)
-?/. - c.4229C>T r.(?) p.(Thr1410Ile)
-?/. - c.4359C>T r.(?) p.(Ile1453=)
?/. - c.4447A>G r.(?) p.(Met1483Val)
?/. - c.4553A>G r.(?) p.(Asp1518Gly)
-?/. - c.4833A>G r.(?) p.(Thr1611=)
?/. - c.5534T>A r.(?) p.(Leu1845His)
-?/. - c.6001T>C r.(?) p.(Ser2001Pro)
-?/. - c.6156A>G r.(?) p.(Leu2052=)
?/. - c.6670G>A r.(?) p.(Ala2224Thr)
-?/. - c.7174A>G r.(?) p.(Ser2392Gly)
?/. - c.7301C>T r.(?) p.(Thr2434Ile)
-?/. - c.7539C>T r.(?) p.(Asp2513=)
-?/. - c.7594C>A r.(?) p.(Leu2532Ile)
-?/. - c.7827A>G r.(?) p.(Ser2609=)
-?/. - c.7933C>T r.(?) p.(Pro2645Ser)
?/. - c.8855C>T r.(?) p.(Ser2952Leu)
-?/. - c.9181A>G r.(?) p.(Met3061Val)
-?/. - c.9711C>T r.(?) p.(Pro3237=)
-?/. - c.9902C>T r.(?) p.(Pro3301Leu)
-?/. - c.10131C>T r.(?) p.(Asn3377=)
-?/. - c.10560A>G r.(?) p.(Ser3520=)
-?/. - c.10730C>T r.(?) p.(Thr3577Ile)
-?/. - c.10876G>C r.(?) p.(Asp3626His)
?/. - c.11099C>G r.(?) p.(Thr3700Arg)
?/. - c.11646C>G r.(?) p.(Ile3882Met)
-?/. - c.12382A>G r.(?) p.(Arg4128Gly)
-?/. - c.12641G>A r.(?) p.(Gly4214Asp)
?/. - c.12692C>T r.(?) p.(Thr4231Ile)
-?/. - c.12749C>T r.(?) p.(Thr4250Met)
?/. - c.12790G>A r.(?) p.(Gly4264Ser)
?/. - c.13312_13323dup r.(?) p.(Asp4438_Trp4441dup)
?/. - c.13591A>T r.(?) p.(Ile4531Phe)
-?/. - c.14975A>G r.(?) p.(Asp4992Gly)
-?/. - c.15139C>T r.(?) p.(Pro5047Ser)
-?/. - c.15477T>G r.(?) p.(Thr5159=)
?/. - c.15614C>T r.(?) p.(Thr5205Met)
?/. - c.16403C>T r.(?) p.(Thr5468Ile)
-?/. - c.16505C>G r.(?) p.(Thr5502Arg)
-?/. - c.16838C>G r.(?) p.(Thr5613Ser)
-?/. - c.17535C>T r.(?) p.(Thr5845=)
?/. - c.17753C>G r.(?) p.(Pro5918Arg)
?/. - c.17774G>A r.(?) p.(Ser5925Asn)
-?/. - c.17878C>T r.(?) p.(Leu5960Phe)
-?/. - c.17982C>T r.(?) p.(Leu5994=)
?/. - c.18241_18242del r.(?) p.(Asp6081Glnfs*26)
-?/. - c.18542C>A r.(?) p.(Ala6181Glu)
-?/. - c.18869C>T r.(?) p.(Thr6290Ile)
-?/. - c.18991G>A r.(?) p.(Ala6331Thr)
-?/. - c.19055C>T r.(?) p.(Ala6352Val)
?/. - c.19369C>T r.(?) p.(Gln6457*)
-?/. - c.19387G>A r.(?) p.(Asp6463Asn)
?/. - c.19590A>T r.(?) p.(Leu6530Phe)
-?/. - c.19915C>T r.(?) p.(Pro6639Ser)
-?/. - c.20087C>T r.(?) p.(Ser6696Phe)
-?/. - c.21981G>A r.(?) p.(Lys7327=)
?/. - c.23008C>T r.(?) p.(Pro7670Ser)
-?/. - c.23085C>T r.(?) p.(Ala7695=)
-?/. - c.23220C>A r.(?) p.(Thr7740=)
?/. - c.23584G>A r.(?) p.(Glu7862Lys)
?/. - c.24227C>G r.(?) p.(Ala8076Gly)
-?/. - c.24373A>G r.(?) p.(Lys8125Glu)
-?/. - c.24983C>A r.(?) p.(Thr8328Asn)
-?/. - c.25105G>A r.(?) p.(Val8369Ile)
?/. - c.25606A>G r.(?) p.(Met8536Val)
-?/. - c.25909G>A r.(?) p.(Glu8637Lys)
?/. - c.26348C>G r.(?) p.(Ala8783Gly)
-?/. - c.26762C>A r.(?) p.(Ala8921Asp)
?/. - c.26878C>T r.(?) p.(Pro8960Ser)
?/. - c.28064C>T r.(?) p.(Thr9355Ile)
-?/. - c.28066C>T r.(?) p.(Pro9356Ser)
?/. - c.28957A>G r.(?) p.(Ile9653Val)
?/. - c.29465C>T r.(?) p.(Ser9822Phe)
-?/. - c.30235A>T r.(?) p.(Thr10079Ser)
-?/. - c.30935C>T r.(?) p.(Pro10312Leu)
?/. - c.30991C>T r.(?) p.(Pro10331Ser)
-?/. - c.31490G>C r.(?) p.(Ser10497Thr)
-?/. - c.31572G>T r.(?) p.(Met10524Ile)
-?/. - c.31760A>T r.(?) p.(Asp10587Val)
-?/. - c.31976C>T r.(?) p.(Ser10659Leu)
?/. - c.32435C>G r.(?) p.(Thr10812Arg)
-?/. - c.32504T>C r.(?) p.(Val10835Ala)
-?/. - c.34262C>A r.(?) p.(Thr11421Asn)
?/. - c.34547C>G r.(?) p.(Thr11516Ser)
-?/. - c.34625T>C r.(?) p.(Met11542Thr)
?/. - c.34666G>A r.(?) p.(Asp11556Asn)
-?/. - c.34760C>T r.(?) p.(Thr11587Met)
-?/. - c.34972A>G r.(?) p.(Thr11658Ala)
-?/. - c.35326A>C r.(?) p.(Thr11776Pro)
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