Variant #0000605622 (NC_000001.10:g.26378395_26378396del, NC_000001.10(NM_032588.3):c.1052-21_1052-20del (TRIM63))

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.26378395_26378396del
DNA change (hg38) g.26051904_26051905del
Published as TRIM63(NM_032588.3):c.1052-21_1052-20delGT
ISCN -
DB-ID SLC30A2_000002 See all 2 reported entries
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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC30A2 NM_032513.3 -?/. - c.-6008_-6007del r.(?) p.(=)
TRIM63 NM_032588.3 -?/. - c.1052-21_1052-20del r.(=) p.(=)


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