Variant #0000964653 (NC_000007.13:g.69064650C>T, NM_015570.2:c.11C>T (AUTS2))

Chromosome 7
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.69064650C>T
DNA change (hg38) -
Published as AUTS2(NM_001127231.1):c.11C>T (p.(Pro4Leu)), AUTS2(NM_001127231.2):c.11C>T (p.P4L), AUTS2(NM_001127231.3):c.11C>T (p.P4L), AUTS2(NM_015570.4):c.11C...
ISCN -
DB-ID AUTS2_000016 See all 4 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) 0.00343 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +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     
AUTS2 NM_015570.2 ?/. - c.11C>T r.(?) p.(Pro4Leu)


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