Variant #0000545745 (NC_000011.9:g.75141426_75141434dup, NM_030792.6:c.*5129_*5137dup (GDPD5))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.75141426_75141434dup
DNA change (hg38) g.75430381_75430389dup
Published as KLHL35(NM_001039548.2):c.252_260dupGGTGCCAGT (p.V85_V87dup)
ISCN -
DB-ID GDPD5_000003
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KLHL35 NM_001039548.2 ?/. - c.252_260dup r.(?) p.(Val85_Val87dup)
GDPD5 NM_030792.6 ?/. - c.*5129_*5137dup r.(=) p.(=)


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