Variant #0000281387 (NC_000012.11:g.121437221T>C, NC_000012.11(NM_000545.5):c.1623+29T>C (HNF1A))

Chromosome 12
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.121437221T>C
DNA change (hg38) g.120999418T>C
Published as HNF1A(NM_000545.8):c.1623+29T>C
ISCN -
DB-ID HNF1A_000064 See all 551 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) 0.82303 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNF1A NM_000545.5 -/. - c.1623+29T>C r.(=) p.(=)
C12orf43 NM_022895.1 -/. - c.*4735A>G r.(=) p.(=)


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