Unique variants in gene KLF11

Information The variants shown are described using the NM_003597.4 transcript reference sequence.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
?/. 1 - c.42+16_42+29dup VUS r.(=) p.(=) g.10183901_10183914dup - KLF11(NM_001177716.1):c.-126_-125insCTGCCGCGGCGGGA (p.(=)) - KLF11_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
-/. 1 - c.185A>G benign r.(?) p.(Gln62Arg) g.10186419A>G - KLF11(NM_001177718.1):c.134A>G (p.Q45R) - KLF11_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
-?/. 1 - c.659C>T likely benign r.(?) p.(Thr220Met) g.10188123C>T - KLF11(NM_001177716.1):c.608C>T (p.(Thr203Met)) - KLF11_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
?/. 1 - c.703T>G VUS r.(?) p.(Leu235Val) g.10188167T>G - KLF11(NM_001177716.1):c.652T>G (p.(Leu218Val)) - KLF11_000009 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
?/. 1 - c.1146T>G VUS r.(?) p.(Cys382Trp) g.10188610T>G - KLF11(NM_001177716.1):c.1095T>G (p.(Cys365Trp)) - KLF11_000013 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
-/. 1 - c.1185A>T benign r.(?) p.(=) g.10188649A>T - KLF11(NM_001177718.1):c.1134A>T (p.V378=) - KLF11_000019 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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