Variant #0000271199 (NC_000001.10:g.29442328C>T, NC_000001.10(NM_203342.2):c.*6+13C>T (EPB41))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.29442328C>T
DNA change (hg38) g.29115816C>T
Published as EPB41(NM_203342.2):c.*6+13C>T
ISCN -
DB-ID EPB41_000021
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) 0.0079 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
TMEM200B NM_001003682.3 -/. - c.*5089G>A r.(=) p.(=)
EPB41 NM_203342.2 -/. - c.*6+13C>T r.(=) p.(=)


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