Variant #0000619201 (NC_000023.10:g.153214810G>A, NM_005334.2:c.6096C>T (HCFC1))

Chromosome X
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.153214810G>A
DNA change (hg38) g.153949359G>A
Published as HCFC1(NM_005334.2):c.6096C>T (p.A2032=)
ISCN -
DB-ID HCFC1_000081
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-21 14:01:05 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RENBP NM_002910.5 -?/. - c.-4748C>T r.(?) p.(=)
HCFC1 NM_005334.2 -?/. - c.6096C>T r.(?) p.(Ala2032=)


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