Variant #0000568875 (NC_000019.9:g.7965792_7965794del, NM_145185.2:c.-3038_-3036del (MAP2K7))

Chromosome 19
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.7965792_7965794del
DNA change (hg38) g.7900907_7900909del
Published as LRRC8E(NM_001268284.1):c.2379_2381del (p.(Glu795del))
ISCN -
DB-ID MAP2K7_000002
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 2020-07-15 11:14:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC8E NM_025061.4 -?/. - c.2385_2387del r.(?) p.(Glu796Ter)
MAP2K7 NM_145185.2 -?/. - c.-3038_-3036del r.(?) p.(=)


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