Transcript #00000013 (NM_000179.2, MSH6 gene)

Transcript name mutS homolog 6 (E. coli), transcript variant 1
Gene name MSH6 (mutS homolog 6)
Chromosome 2
Transcript - NCBI ID NM_000179.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000170.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2016-07-08 10:28:55 +00:00 (UTC)
Date last edited N/A


Variants

17 entries on 1 page. Showing entries 1 - 17.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Class     
+?/+? 1 c.59C>T r.(?) p.(Ala20Val) VUS
?/? 1 c.109G>T r.(?) p.(Ala37Ser) VUS
?/? 2 c.267C>G r.(?) p.(Asp89Glu) VUS
+/+ 2 c.402dup r.(?) p.(Asp135*) pathogenic
?/? 4 c.663A>C r.(?) p.(Glu221Asp) VUS
+/+ 4 c.694C>T r.(?) p.(Gln232*) pathogenic
?/? . c.1007C>G r.(?) p.(Thr336Ser) VUS
+?/+? 4 c.1627A>T r.(?) p.(Lys543*) pathogenic
+/+ 4 c.1691C>A r.(?) p.(Ser564*) pathogenic
+/+ . c.2653A>T r.(?) p.(Lys885*) pathogenic
+/+ 5 c.3202C>T r.(?) p.(Arg1068*) pathogenic
+/+ 5 c.3261dupC r.(?) p.(Phe1088Leufs*5) pathogenic
?/? 5 c.3284G>A r.(?) p.(Arg1095His) VUS
?/- 6 c.3543C>G r.(?) p.(Asp1181Glu) VUS
+/+ 7 c.3573del r.(?) p.(Phe1191Leufs*4) pathogenic
?/? 9 c.3986C>T r.(?) p.(Ser1329Leu) likely benign
-?/-? 10 c.4081dup r.(?) p.(*1361Leuext*2) likely benign
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