Full data view for gene USH1G


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_173477.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

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ClinVar ID     

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VIP     

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?/. - c.1258C>G r.(?) p.(Leu420Val) - Unknown - VUS g.72915673G>C g.74919578G>C USH1G(NM_173477.4):c.1258C>G (p.L420V) - USH1G_000027 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.1258C>G r.(?) p.(Leu420Val) - Unknown - VUS g.72915673G>C g.74919578G>C USH1G(NM_173477.4):c.1258C>G (p.L420V) - USH1G_000027 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/-? 2 c.1258C>G r.(?) p.(Leu420Val) SAM (385-447) Unknown ACMG likely benign g.72915673G>C g.74919578G>C - - USH1G_000027 heterozygous, {USMAUSH1G:L420V} {MSV3dQ495M9:p.Leu420Val} PubMed: Glöcke et al., 2013 - rs139897506 Germline - - +BccI ;-SfaNI; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Glöcke et al., 2013 proband - - - - - - - - 1 Anne-Françoise Roux
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