Variant #0000857516 (NC_000001.10:g.45974471A>T, NM_015506.2:c.433A>T (MMACHC))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45974471A>T
DNA change (hg38) -
Published as MMACHC(NM_001330540.1):c.262A>T (p.(Ile88Leu)), MMACHC(NM_001330540.2):c.262A>T (p.I88L), MMACHC(NM_015506.2):c.433A>T (p.I145L)
ISCN -
DB-ID MMACHC_000044 See all 3 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) 0.00054 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MMACHC NM_015506.2 ?/. - c.433A>T r.(?) p.(Ile145Leu)
PRDX1 NM_181697.2 ?/. - c.*2530T>A r.(=) p.(=)


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