Variant #0000321768 (NC_000010.10:g.115357744C>G, NM_004132.3:c.*9616C>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.115357744C>G
DNA change (hg38) g.113597985C>G
Published as NRAP(NM_001261463.1):c.4316G>C (p.(Gly1439Ala))
ISCN -
DB-ID NRAP_000002
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HABP2 NM_004132.3 ?/. - c.*9616C>G r.(=) p.(=)
NRAP NM_198060.3 ?/. - c.4316G>C r.(?) p.(Gly1439Ala)


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