Variant #0000546668 (NC_000012.11:g.113537871C>A, NM_004658.2:c.2278G>T (RASAL1))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.113537871C>A
DNA change (hg38) g.113100066C>A
Published as RASAL1(NM_004658.2):c.2278G>T (p.A760S)
ISCN -
DB-ID DTX1_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) 0.00095 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DTX1 NM_004416.2 -/. - c.*3127C>A r.(=) p.(=)
RASAL1 NM_004658.2 -/. - c.2278G>T r.(?) p.(Ala760Ser)


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