Variant #0000689552 (NC_000005.9:g.79929740C>T, NM_002439.4:c.-20807C>T (MSH3))

Chromosome 5
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.79929740C>T
DNA change (hg38) -
Published as DHFR(NM_000791.3):c.441G>A (p.T147=), DHFR(NM_000791.4):c.441G>A (p.T147=)
ISCN -
DB-ID DHFR_000067 See all 2 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) 0.00066 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DHFR NM_000791.3 -?/. - c.441G>A r.(?) p.(Thr147=)
MTRNR2L2 NM_001190470.1 -?/. - c.*16079G>A r.(=) p.(=)
MSH3 NM_002439.4 -?/. - c.-20807C>T r.(?) p.(=)


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