Variant #0000623748 (NC_000017.10:g.66339933G>C, NC_000017.10(NM_001267727.1):c.406+1G>C (ARSG))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.66339933G>C
DNA change (hg38) g.68343792G>C
Published as ARSG(NM_001352910.1):c.406+1G>C
ISCN -
DB-ID SLC16A6_000002
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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 +/. - c.406+1G>C r.spl? p.?
SLC16A6 NM_004694.4 +/. - c.-52714C>G r.(?) p.(=)
ARSG NM_014960.3 +/. - c.406+1G>C r.spl? p.?
ARSG NM_014960.4 +/. - c.406+1G>C r.spl? p.?
WIPI1 NM_017983.5 +/. - c.*77981C>G r.(=) p.(=)


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