Variant #0000677046 (NC_000003.11:g.49456754A>G, NM_000481.3:c.635T>C (AMT))

Chromosome 3
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.49456754A>G
DNA change (hg38) -
Published as AMT(NM_000481.3):c.635T>C (p.V212A), AMT(NM_000481.4):c.635T>C (p.V212A)
ISCN -
DB-ID AMT_000019 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) 0.0003 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMT NM_000481.3 -?/. - c.635T>C r.(?) p.(Val212Ala)
TCTA NM_022171.2 -?/. - c.*4459A>G r.(=) p.(=)
NICN1 NM_032316.3 -?/. - c.*5512T>C r.(=) p.(=)


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