Variant #0000726631 (NC_000017.10:g.66303721G>A, NM_001267727.1:c.87G>A (ARSG))

Chromosome 17
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.66303721G>A
DNA change (hg38) -
Published as ARSG(NM_001352903.2):c.87G>A (p.G29=), ARSG(NM_001352910.1):c.87G>A (p.G29=), ARSG(NM_014960.5):c.87G>A (p.G29=)
ISCN -
DB-ID SLC16A6_000001 See all 3 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) 0.00188 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 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 -?/. - c.87G>A r.(?) p.(Gly29=)
SLC16A6 NM_004694.4 -?/. - c.-16502C>T r.(?) p.(=)
ARSG NM_014960.3 -?/. - c.87G>A r.(?) p.(Gly29=)
ARSG NM_014960.4 -?/. - c.87G>A r.(?) p.(Gly29=)
WIPI1 NM_017983.5 -?/. - c.*114193C>T r.(=) p.(=)


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