Variant #0000605657 (NC_000001.10:g.27875559G>C, NM_001029882.2:c.3068C>G (AHDC1))

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.27875559G>C
DNA change (hg38) g.27549048G>C
Published as AHDC1(NM_001029882.2):c.3068C>G (p.(Pro1023Arg)), AHDC1(NM_001029882.3):c.3068C>G (p.P1023R)
ISCN -
DB-ID AHDC1_000046 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AHDC1 NM_001029882.2 -?/. - c.3068C>G r.(?) p.(Pro1023Arg)


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