Variant #0000574475 (NC_000023.10:g.153214809C>T, NM_005334.2:c.6097G>A (HCFC1))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.153214809C>T
DNA change (hg38) g.153949358C>T
Published as HCFC1(NM_005334.2):c.6097G>A (p.(Asp2033Asn))
ISCN -
DB-ID HCFC1_000048
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.-4747G>A r.(?) p.(=)
HCFC1 NM_005334.2 ?/. - c.6097G>A r.(?) p.(Asp2033Asn)


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