Variant #0000539204 (NC_000010.10:g.115405648G>A, NM_004132.3:c.*57520G>A (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.115405648G>A
DNA change (hg38) g.113645889G>A
Published as NRAP(NM_001261463.1):c.1046C>T (p.S349L)
ISCN -
DB-ID HABP2_000012
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) 5.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
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.*57520G>A r.(=) p.(=)
NRAP NM_198060.3 ?/. - c.1046C>T r.(?) p.(Ser349Leu)


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