Variant #0000508549 (NC_000001.10:g.92713561_92713564del, NC_000001.10(NM_053274.2):c.1474-15_1474-12del (GLMN))

Chromosome 1
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.92713561_92713564del
DNA change (hg38) g.92248004_92248007del
Published as GLMN(NM_053274.3):c.1474-15_1474-12delTTTC
ISCN -
DB-ID C1orf146_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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.*2330_*2333del r.(=) p.(=)
RPAP2 NM_024813.2 -?/. - c.-51070_-51067del r.(?) p.(=)
GLMN NM_053274.2 -?/. - c.1474-15_1474-12del r.(=) p.(=)


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