Variant #0000526134 (NC_000005.9:g.79950227G>C, NM_002439.4:c.-320G>C (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.79950227G>C
DNA change (hg38) g.80654408G>C
Published as DHFR(NM_000791.3):c.82C>G (p.(Leu28Val))
ISCN -
DB-ID DHFR_000015
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     
DHFR NM_000791.3 -?/. - c.82C>G r.(?) p.(Leu28Val)
MTRNR2L2 NM_001190470.1 -?/. - c.-4322C>G r.(?) p.(=)
MSH3 NM_002439.4 -?/. - c.-320G>C r.(?) p.(=)


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