Variant #0000281081 (NC_000001.10:g.92712601_92712602del, NC_000001.10(NM_053274.2):c.1668+19_1668+20del (GLMN))

Chromosome 1
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.92712601_92712602del
DNA change (hg38) g.92247044_92247045del
Published as GLMN(NM_053274.3):c.1668+19_1668+20delTT
ISCN -
DB-ID GLMN_000006
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1orf146 NM_001012425.1 -/. - c.*1370_*1371del r.(=) p.(=)
RPAP2 NM_024813.2 -/. - c.-52030_-52029del r.(?) p.(=)
GLMN NM_053274.2 -/. - c.1668+19_1668+20del r.(=) p.(=)


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