Variant #0000507302 (NC_000001.10:g.35453651A>C, NM_007167.3:c.3032T>G (ZMYM6))

Chromosome 1
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.35453651A>C
DNA change (hg38) g.34988050A>C
Published as ZMYM6(NM_007167.4):c.3032T>G (p.F1011C)
ISCN -
DB-ID ZMYM6_000013
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) 0.00333 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZMYM6NB NM_001195156.1 -/. - c.-2745T>G r.(?) p.(=)
ZMYM6 NM_007167.3 -/. - c.3032T>G r.(?) p.(Phe1011Cys)


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