UQCC1 c.464+6630A>G

Variant ID: 20-33947730-T-C

NM_018244.4(UQCC1):c.464+6630A>G

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Joint disease-specificity at the regulatory base-pair level.

Nature Communications
Muthuirulan, Pushpanathan P; Zhao, Dewei D; Young, Mariel M; Richard, Daniel D; Liu, Zun Z; Emami, Alireza A; Portilla, Gabriela G; Hosseinzadeh, Shayan S; Cao, Jiaxue J; Maridas, David D; Sedlak, Mary M; Menghini, Danilo D; Cheng, Liangliang L; Li, Lu L; Ding, Xinjia X; Ding, Yan Y; Rosen, Vicki V; Kiapour, Ata M AM; Capellini, Terence D TD
Publication Date: 2021-07-06

Variant appearance in text: rs735531
PubMed Link: 34230488
Variant Present in the following documents:
  • 41467_2021_24345_MOESM1_ESM.pdf
View BVdb publication page


Joint disease-specificity at the regulatory base-pair level.

Nature Communications
Muthuirulan, Pushpanathan P; Zhao, Dewei D; Young, Mariel M; Richard, Daniel D; Liu, Zun Z; Emami, Alireza A; Portilla, Gabriela G; Hosseinzadeh, Shayan S; Cao, Jiaxue J; Maridas, David D; Sedlak, Mary M; Menghini, Danilo D; Cheng, Liangliang L; Li, Lu L; Ding, Xinjia X; Ding, Yan Y; Rosen, Vicki V; Kiapour, Ata M AM; Capellini, Terence D TD
Publication Date: 2021-07-06

Variant appearance in text: rs735531
PubMed Link: 34230488
Variant Present in the following documents:
  • 41467_2021_24345_MOESM1_ESM.pdf
View BVdb publication page