Variant #0000893391 (NC_000017.10:g.19261160G>C, NM_015681.3:c.237C>G (B9D1))

Chromosome 17
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.19261160G>C
DNA change (hg38) -
Published as B9D1(NM_001243473.2):c.296C>G (p.P99R)
ISCN -
DB-ID EPN2_000006
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) 0.00068 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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPN2 NM_014964.4 -?/. - c.*23593G>C r.(=) p.(=)
B9D1 NM_015681.3 -?/. - c.237C>G r.(?) p.(Pro79=)
MAPK7 NM_139033.2 -?/. - c.-20260G>C r.(?) p.(=)


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