Variant #0000289140 (NC_000012.11:g.54675752_54675754del, NC_000012.11(NM_031157.2):c.279+27_279+29del (HNRNPA1))

Chromosome 12
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.54675752_54675754del
DNA change (hg38) g.54281968_54281970del
Published as HNRNPA1(NM_031157.3):c.279+27_279+29delTTC, HNRNPA1(NM_031157.4):c.279+27_279+29delCTT
ISCN -
DB-ID HNRNPA1_000005 See all 2 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
CBX5 NM_012117.2 -?/. - c.-1994_-1992del r.(?) p.(=)
HNRNPA1 NM_031157.2 -?/. - c.279+27_279+29del r.(=) p.(=)


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