Variant #0000605224 (NC_000001.10:g.226034856_226034858dup, NM_014698.2:c.2323_2325dup (TMEM63A))

Chromosome 1
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.226034856_226034858dup
DNA change (hg38) g.225847155_225847157dup
Published as TMEM63A(NM_014698.2):c.2325_2326insCAG (p.(Gln775dup))
ISCN -
DB-ID TMEM63A_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +01:00 (CET)
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     
EPHX1 NM_000120.3 -?/. - c.*1808_*1810dup r.(=) p.(=)
TMEM63A NM_014698.2 -?/. - c.2323_2325dup r.(?) p.(Gln775dup)


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