Variant #0000529972 (NC_000006.11:g.87994211_87994215del, NM_198568.2:c.418_422del (GJB7))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.87994211_87994215del
DNA change (hg38) g.87284493_87284497del
Published as GJB7(NM_198568.2):c.418_422del (p.(Val140IlefsTer3))
ISCN -
DB-ID GJB7_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-19 15:18:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMIM8 NM_020425.4 -?/. - c.-38163_-38159del r.(?) p.(=)
GJB7 NM_198568.2 -?/. - c.418_422del r.(?) p.(Val140IlefsTer3)


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