All variants in the NLGN3 gene

Information The variants shown are described using the NM_018977.3 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

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     
-/. - c.-3855_-3844dup r.(?) p.(=) - benign g.70361160_70361171dup g.71141310_71141321dup MED12(NM_005120.2):c.6339_6340insCAGCAACACCAG (p.(His2116_Gln2119dup)), MED12(NM_005120.2):c.6348_6359dupCCAGCAGCAACA (p.H2116_Q2119dup), MED12(NM...) - MED12_000118 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Groningen
-/. - c.-3855_-3844dup r.(?) p.(=) - benign g.70361160_70361171dup g.71141310_71141321dup MED12(NM_005120.2):c.6339_6340insCAGCAACACCAG (p.(His2116_Gln2119dup)), MED12(NM_005120.2):c.6348_6359dupCCAGCAGCAACA (p.H2116_Q2119dup), MED12(NM...) - MED12_000118 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-?/. - c.-3855_-3844dup r.(?) p.(=) - likely benign g.70361160_70361171dup g.71141310_71141321dup MED12(NM_005120.2):c.6339_6340insCAGCAACACCAG (p.(His2116_Gln2119dup)), MED12(NM_005120.2):c.6348_6359dupCCAGCAGCAACA (p.H2116_Q2119dup), MED12(NM...) - MED12_000118 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Utrecht
-?/. - c.-3855_-3844dup r.(?) p.(=) - likely benign g.70361160_70361171dup g.71141310_71141321dup MED12(NM_005120.2):c.6339_6340insCAGCAACACCAG (p.(His2116_Gln2119dup)), MED12(NM_005120.2):c.6348_6359dupCCAGCAGCAACA (p.H2116_Q2119dup), MED12(NM...) - MED12_000118 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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