Variant #0001014591 (NC_000010.10:g.115380419C>T, NM_004132.3:c.*32291C>T (HABP2))

Chromosome 10
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.115380419C>T
DNA change (hg38) -
Published as NRAP(NM_001261463.1):c.2818G>A (p.A940T), NRAP(NM_001261463.2):c.2818G>A (p.A940T)
ISCN -
DB-ID NRAP_000008 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) 0.00135 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HABP2 NM_004132.3 -?/. - c.*32291C>T r.(=) p.(=)
NRAP NM_198060.3 -?/. - c.2818G>A r.(?) p.(Ala940Thr)


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