Variant #0000606360 (NC_000002.11:g.176957818_176957819insTGC, NM_000523.3:c.200_201insTGC (HOXD13))

Chromosome 2
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.176957818_176957819insTGC
DNA change (hg38) g.176093090_176093091insTGC
Published as HOXD13(NM_000523.3):c.198_199insGCT (p.(Ala66dup))
ISCN -
DB-ID HOXD13_000021
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXD13 NM_000523.3 -?/. - c.200_201insTGC r.(?) p.(Ala71dup)


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