Variant #0000857108 (NC_000001.10:g.161192511C>G, NM_004106.1:c.*3778C>G (FCER1G))

Chromosome 1
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.161192511C>G
DNA change (hg38) -
Published as APOA2(NM_001643.1):c.185+197G>C
ISCN -
DB-ID APOA2_000014
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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NR1I3 NM_001077469.2 -/. - c.*6961G>C r.(=) p.(=)
APOA2 NM_001643.1 -/. - c.185+197G>C r.(=) p.(=)
FCER1G NM_004106.1 -/. - c.*3778C>G r.(=) p.(=)
NR1I3 NM_005122.4 -/. - c.*7076G>C r.(=) p.(=)
TOMM40L NM_032174.4 -/. - c.-3551C>G r.(?) p.(=)


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