Variant #0000543317 (NC_000011.9:g.18269516T>C, NM_030754.4:c.43A>G (SAA2))

Chromosome 11
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.18269516T>C
DNA change (hg38) g.18247969T>C
Published as SAA2(NM_001127380.2):c.43A>G (p.(Ser15Gly))
ISCN -
DB-ID SAA2_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
SAA2-SAA4 NM_001199744.1 -?/. - c.43A>G r.(?) p.(Ser15Gly)
SAA4 NM_006512.3 -?/. - c.-11257A>G r.(?) p.(=)
SAA2 NM_030754.4 -?/. - c.43A>G r.(?) p.(Ser15Gly)


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