Variant #0000505936 (NC_000001.10:g.2343940A>G, NM_153818.1:c.2T>C (PEX10))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2343940A>G
DNA change (hg38) g.2412501A>G
Published as PEX10(NM_153818.1):c.2T>C (p.M1?)
ISCN -
DB-ID PEX10_000024 See all 2 reported entries
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 2020-09-08 13:47:08 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RER1 NM_007033.4 +?/. - c.*9377A>G r.(=) p.(=)
PEX10 NM_153818.1 +?/. - c.2T>C r.(?) p.(Met1?)


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