Variant #0000978906 (NC_000010.10:g.115405588C>G, NM_004132.3:c.*57460C>G (HABP2))

Chromosome 10
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.115405588C>G
DNA change (hg38) -
Published as NRAP(NM_198060.4):c.1106G>C (p.(Ser369Thr))
ISCN -
DB-ID HABP2_000034
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HABP2 NM_004132.3 ?/. - c.*57460C>G r.(=) p.(=)
NRAP NM_198060.3 ?/. - c.1106G>C r.(?) p.(Ser369Thr)


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