Variant #0000886980 (NC_000006.11:g.10874572_10874580dup, NM_004752.3:c.1177_1185dup (GCM2))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.10874572_10874580dup
DNA change (hg38) -
Published as GCM2(NM_004752.4):c.1177_1185dupGCCTACCAG (p.A393_Q395dup)
ISCN -
DB-ID GCM2_000007
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCM2 NM_004752.3 -/. - c.1177_1185dup r.(?) p.(Ala393_Gln395dup)


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