Variant #0000535216 (NC_000008.10:g.6302736G>C, NM_001118887.1:c.*57886C>G (ANGPT2))

Chromosome 8
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.6302736G>C
DNA change (hg38) g.6445215G>C
Published as MCPH1(NM_001322042.1):c.1493G>C (p.C498S)
ISCN -
DB-ID ANGPT2_000011
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 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 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANGPT2 NM_001118887.1 -?/. - c.*57886C>G r.(=) p.(=)
MCPH1 NM_024596.2 -?/. - c.1493G>C r.(?) p.(Cys498Ser)
MCPH1 NM_024596.3 -?/. - c.1493G>C r.(?) p.(Cys498Ser)


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