Variant #0000619200 (NC_000023.10:g.153209869T>C, NM_005334.2:c.*4929A>G (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.153209869T>C
DNA change (hg38) g.153944417T>C
Published as RENBP(NM_002910.5):c.29A>G (p.(Asp10Gly)), RENBP(NM_002910.6):c.29A>G (p.D10G)
ISCN -
DB-ID HCFC1_000046 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) 0.00107 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.29A>G r.(?) p.(Asp10Gly)
HCFC1 NM_005334.2 -?/. - c.*4929A>G r.(=) p.(=)


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