Variant #0000564603 (NC_000018.9:g.29172937G>A, NM_000371.3:c.148G>A (TTR))

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.29172937G>A
DNA change (hg38) g.31592974G>A
Published as TTR(NM_000371.3):c.148G>A (p.V50M, p.(Val50Met)), TTR(NM_000371.4):c.148G>A (p.V50M)
ISCN -
DB-ID TTR_000011 See all 38 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) 0.0001 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTR NM_000371.3 +/. - c.148G>A r.(?) p.(Val50Met)


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