Variant #0000525816 (NC_000005.9:g.52394439T>C, NM_176806.3:c.*480A>G (MOCS2))

Chromosome 5
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.52394439T>C
DNA change (hg38) g.53098609T>C
Published as MOCS2(NM_004531.5):c.560A>G (p.N187S)
ISCN -
DB-ID ITGA2_000016
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) 0.00086 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITGA2 NM_002203.3 -?/. - c.*8010T>C r.(=) p.(=)
MOCS2 NM_004531.4 -?/. - c.560A>G r.(?) p.(Asn187Ser)
MOCS2 NM_176806.3 -?/. - c.*480A>G r.(=) p.(=)


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