Variant #0000857518 (NC_000001.10:g.45974804_45974809del, NM_015506.2:c.766_771del (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.45974804_45974809del
DNA change (hg38) -
Published as MMACHC(NM_001330540.1):c.595_600del (p.(Ala199_Pro200del)), MMACHC(NM_015506.2):c.766_771delGCCCCC (p.A256_P257del)
ISCN -
DB-ID MMACHC_000046 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MMACHC NM_015506.2 ?/. - c.766_771del r.(?) p.(Ala256_Pro257del)
PRDX1 NM_181697.2 ?/. - c.*2195_*2200del r.(=) p.(=)


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