Variant #0000609732 (NC_000005.9:g.41150035A>G, NC_000005.9(NM_000065.2):c.2381+2T>C (C6))

Chromosome 5
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.41150035A>G
DNA change (hg38) g.41149933A>G
Published as C6(NM_000065.2):c.2381+2T>C, C6(NM_001115131.2):c.2381+2T>C, C6(NM_001115131.4):c.2381+2T>C
ISCN -
DB-ID C6_000008 See all 5 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) 0.00218 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C6 NM_000065.2 +?/. - c.2381+2T>C r.spl? p.?


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