Transcript #00014071 (NM_018406.6, MUC4 gene)

Transcript name transcript variant 1
Gene name MUC4 (mucin 4, cell surface associated)
Chromosome 3
Transcript - NCBI ID NM_018406.6
Transcript - Ensembl ID -
Protein - NCBI ID NP_060876.5
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

69 entries on 1 page. Showing entries 1 - 69.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.203A>G r.(?) p.(Gln68Arg)
-?/. - c.320T>C r.(?) p.(Val107Ala)
-?/. - c.384C>A r.(?) p.(Thr128=)
-?/. - c.418A>G r.(?) p.(Met140Val)
-?/. - c.759C>G r.(?) p.(Val253=)
-?/. - c.1037C>T r.(?) p.(Pro346Leu)
?/. - c.2209G>A r.(?) p.(Ala737Thr)
-?/. - c.2214T>C r.(?) p.(Leu738=)
?/. - c.2399C>T r.(?) p.(Ala800Val)
-?/. - c.3050T>A r.(?) p.(Val1017Glu)
-?/. - c.3461A>C r.(?) p.(His1154Pro)
-/. - c.3996T>C r.(?) p.(Thr1332=)
?/. - c.4030C>T r.(?) p.(Pro1344Ser)
-?/. - c.4093del r.(?) p.(Asp1365Metfs*79)
-?/. - c.4095del r.(?) p.(Asp1365Glufs*79)
-?/. - c.4870T>G r.(?) p.(Ser1624Ala)
-?/. - c.5306T>C r.(?) p.(Val1769Ala)
-?/. - c.5946C>A r.(?) p.(Ala1982=)
-?/. - c.6030T>G r.(?) p.(Ser2010=)
-?/. - c.6044C>G r.(?) p.(Thr2015Ser)
-?/. - c.6095C>T r.(?) p.(Pro2032Leu)
-?/. - c.6141C>G r.(?) p.(Thr2047=)
-?/. - c.6208C>G r.(?) p.(Pro2070Ala)
-?/. - c.6423C>T r.(?) p.(Asp2141=)
-?/. - c.6637A>G r.(?) p.(Ser2213Gly)
-?/. - c.6997G>C r.(?) p.(Asp2333His)
-?/. - c.7000A>G r.(?) p.(Thr2334Ala)
-?/. - c.7499C>G r.(?) p.(Thr2500Ser)
-?/. - c.7541C>A r.(?) p.(Pro2514His)
?/. - c.7666G>A r.(?) p.(Gly2556Ser)
-?/. - c.7981_8124del r.(?) p.(Ser2661_Thr2708del)
-?/. - c.8055T>G r.(?) p.(His2685Gln)
-?/. - c.8110_8253del r.(?) p.(Ser2704_Thr2751del)
-?/. - c.8141A>C r.(?) p.(Tyr2714Ser)
-?/. - c.8224A>G r.(?) p.(Thr2742Ala)
-/. - c.8366G>A r.(?) p.(Ser2789Asn)
-?/. - c.8477_8572del r.(?) p.(Phe2826_Val2857del)
?/. - c.8487T>G r.(?) p.(His2829Gln)
-?/. - c.8936_9031del r.(?) p.(Asp2979_Pro3010del)
-?/. - c.9819A>T r.(?) p.(Ala3273=)
-?/. - c.9914_10009del r.(?) p.(Val3305_Ser3336del)
?/. - c.9997A>G r.(?) p.(Ser3333Gly)
?/. - c.9998G>A r.(?) p.(Ser3333Asn)
?/. - c.10000C>A r.(?) p.(Pro3334Thr)
-?/. - c.10004C>T r.(?) p.(Ser3335Phe)
-?/. - c.10116T>A r.(?) p.(Gly3372=)
-?/. - c.10313C>T r.(?) p.(Ala3438Val)
?/. - c.10324C>G r.(?) p.(Pro3442Ala)
-?/. - c.10430G>T r.(?) p.(Ser3477Ile)
?/. - c.10589C>A r.(?) p.(Ser3530Tyr)
?/. - c.10990C>T r.(?) p.(Pro3664Ser)
-?/. - c.11093C>A r.(?) p.(Pro3698His)
-?/. - c.11127C>G r.(?) p.(His3709Gln)
-?/. - c.11175C>T r.(?) p.(His3725=)
?/. - c.11282T>C r.(?) p.(Leu3761Pro)
?/. - c.11362G>A r.(?) p.(Gly3788Ser)
-?/. - c.11368A>T r.(?) p.(Thr3790Ser)
-?/. - c.11387C>G r.(?) p.(Thr3796Ser)
-/. - c.11977_11979del r.(?) p.(Val3993del)
?/. - c.12101C>A r.(?) p.(Pro4034His)
?/. - c.12491_12630del r.(?) p.(Thr4164Serfs*103)
-?/. - c.12516T>G r.(?) p.(Gly4172=)
-?/. - c.12553G>T r.(?) p.(Ala4185Ser)
-?/. - c.13396G>A r.(?) p.(Gly4466Arg)
?/. - c.13855G>A r.(?) p.(Val4619Met)
-?/. - c.14304C>T r.(?) p.(Asn4768=)
-?/. - c.14969C>G r.(?) p.(Thr4990Ser)
-?/. - c.15216G>A r.(?) p.(Glu5072=)
-?/. - c.15285G>C r.(?) p.(Glu5095Asp)
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