Variant #0000286648 (NC_000006.11:g.84798956G>A, NM_138409.2:c.374G>A (MRAP2))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.84798956G>A
DNA change (hg38) g.84089237G>A
Published as MRAP2(NM_001346542.2):c.374G>A (p.R125H), MRAP2(NM_138409.4):c.374G>A (p.R125H)
ISCN -
DB-ID MRAP2_000003 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) 0.00141 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
MRAP2 NM_138409.2 -/. - c.374G>A r.(?) p.(Arg125His)


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