Variant #0000950286 (NC_000014.8:g.75515951A>G, NM_001040108.1:c.408T>C (MLH3))

Chromosome 14
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.75515951A>G
DNA change (hg38) -
Published as MLH3(NM_001040108.1):c.408T>C (p.(Asp136=)), MLH3(NM_001040108.2):c.408T>C (p.D136=)
ISCN -
DB-ID MLH3_000004 See all 5 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) 0.00509 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH3 NM_001040108.1 -?/. - c.408T>C r.(?) p.(Asp136=)
ACYP1 NM_001107.3 -?/. - c.*4196T>C r.(=) p.(=)


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