Variant #0000505910 (NC_000001.10:g.2319709C>T, PEX10(NM_153818.1):c.*17496G>A)

Chromosome 1
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.2319709C>T
DNA change (hg38) g.2388270C>T
Published as MORN1(NM_024848.3):c.216G>A (p.T72=)
ISCN -
DB-ID MORN1_000004
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RER1 NM_007033.4 -?/. - c.-3696C>T r.(?) p.(=)
MORN1 NM_024848.1 -?/. - c.216G>A r.(?) p.(Thr72=)
PEX10 NM_153818.1 -?/. - c.*17496G>A r.(=) p.(=)