Variant #0000327061 (NC_000002.11:g.70524451C>T, NM_032822.2:c.387G>A (FAM136A))

Chromosome 2
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.70524451C>T
DNA change (hg38) g.70297319C>T
Published as FAM136A(NM_001329752.1):c.708G>A (p.(Met236Ile))
ISCN -
DB-ID FAM136A_000011
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNRPG NM_003096.2 -?/. - c.-3670G>A r.(?) p.(=)
FAM136A NM_032822.2 -?/. - c.387G>A r.(?) p.(Met129Ile)


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