Variant #0000717449 (NC_000001.10:g.36557625T>C, NM_017825.2:c.631T>C (ADPRHL2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.36557625T>C
DNA change (hg38) -
Published as ADPRHL2(NM_017825.3):c.631T>C (p.F211L)
ISCN -
DB-ID ADPRHL2_000022
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) 0 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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     
COL8A2 NM_005202.2 ?/. - c.*5545A>G r.(=) p.(=)
TEKT2 NM_014466.2 ?/. - c.*3838T>C r.(=) p.(=)
ADPRHL2 NM_017825.2 ?/. - c.631T>C r.(?) p.(Phe211Leu)


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