Variant #0000680991 (NC_000017.10:g.66339812C>G, NM_001267727.1:c.286C>G (ARSG))

Chromosome 17
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.66339812C>G
DNA change (hg38) -
Published as ARSG(NM_001352910.1):c.286C>G (p.L96V)
ISCN -
DB-ID SLC16A6_000004
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 ?/. - c.286C>G r.(?) p.(Leu96Val)
SLC16A6 NM_004694.4 ?/. - c.-52593G>C r.(?) p.(=)
ARSG NM_014960.3 ?/. - c.286C>G r.(?) p.(Leu96Val)
ARSG NM_014960.4 ?/. - c.286C>G r.(?) p.(Leu96Val)
WIPI1 NM_017983.5 ?/. - c.*78102G>C r.(=) p.(=)


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