http://identifiers.org/hco/1/GRCh38#175067857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159981123-C-A

175067857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 5 prime UTR variant
orthologous variants: 159981123-C-T

175067983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159981001-G-A

http://identifiers.org/hco/1/GRCh38#175067994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159980990-A-C

http://identifiers.org/hco/1/GRCh38#175068015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159980975-C-A

175068386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159980684-T-C

175068445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159980623-A-G

175069015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159980391-G-A

175069015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159980391-G-C

175069155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159980277-A-G

175069317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159980213-A-T

175069329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159980199-C-G

175069699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159979893-A-G

175069807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159979786-G-A

175069807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159979786-G-T

175069939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159979657-T-G

175070256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159979335-A-T

175070577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159979051-T-C

175070809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159978851-T-A

175070809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159978851-T-C

175071093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159978578-T-C

175071248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159978426-G-T

175071256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159978418-T-A

175071256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159978418-T-C

175071362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159978322-G-A

http://identifiers.org/hco/1/GRCh38#175071422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159978267-C-A

175071422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159978267-C-G

175071521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159978185-C-T

175071664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159977979-C-T

http://identifiers.org/hco/1/GRCh38#175072155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159977516-C-A

175072168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159977503-G-A

http://identifiers.org/hco/1/GRCh38#175072575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159977178-C-A

175072601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 159977150-G-A

175072606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 159977145-C-T

175072620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 159977131-G-A

175072700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 159977055-T-C

175072807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 159976951-G-A

175072974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 159976800-A-T

175073109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, missense_variant
orthologous variants: 159976658-G-A

175073263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159976534-T-C

175073273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159976524-C-T

175073278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159976519-G-C

175073528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159976318-T-A

175073598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159976245-G-A

http://identifiers.org/hco/1/GRCh38#175073649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159976191-C-A

175074120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159976065-G-C

http://identifiers.org/hco/1/GRCh38#175074127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159976058-C-A

http://identifiers.org/hco/1/GRCh38#175077340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159975504-C-A

http://identifiers.org/hco/1/GRCh38#175077346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159975498-A-C

175077346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159975498-A-T

175077355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159975489-G-A

175077355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159975489-G-T

175077370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159975474-G-A

175077407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 159975433-G-A

175077407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 159975433-G-C

175077599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975243-G-C

175077623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975219-G-A

175077626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975216-G-A

175077626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975216-G-C

175077653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975189-A-G

175077653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975189-A-T

http://identifiers.org/hco/1/GRCh38#175077686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159975156-A-C

175077686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975156-A-G

175077686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975156-A-T

175077709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: synonymous variant
orthologous variants: 159975133-G-A

175077794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975048-T-A

175077794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975048-T-C

175077794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975048-T-G

175077818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975024-G-A

175077818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159975024-G-C

http://identifiers.org/hco/1/GRCh38#175077856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159974986-C-A

175077856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159974986-C-T

175077908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159974937-G-A

http://identifiers.org/hco/1/GRCh38#175077921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159974924-C-A

175077947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159974898-G-T

175078283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159974647-C-T

175078558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159974507-C-T

175078853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159974309-G-T

http://identifiers.org/hco/1/GRCh38#175079202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159974038-A-C

175079202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159974038-A-G

175079241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159974019-G-T

http://identifiers.org/hco/1/GRCh38#175079287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159973984-C-A

175079287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159973984-C-G

175079287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159973984-C-T

175079366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159973921-T-C

175079467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159973820-G-A

175079467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159973820-G-T

175079490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159973797-T-A

175079490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: synonymous variant
orthologous variants: 159973797-T-C

175079712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159973575-G-T

175079713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159973574-A-G

175079724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159973563-G-A

175079724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159973563-G-T

175079792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159973490-G-A

175079792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159973490-G-T

175080103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159972890-A-T

175080133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159972852-C-G

175080133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159972852-C-T

175080166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159972811-T-C

175080303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159972674-G-A

http://identifiers.org/hco/1/GRCh38#175080372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159972605-C-A

175080372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159972605-C-T

175081446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159970571-C-T

175081460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159970557-C-T

175081734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159970337-C-T

175082273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159969766-G-A

175082294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159969745-G-C

175082983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159969078-G-T

175083069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968997-C-G

175083095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968971-G-A

175083277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968791-T-C

175083484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968605-G-A

http://identifiers.org/hco/1/GRCh38#175083498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159968592-A-C

175083517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968573-G-T

175083520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968570-G-A

175083581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968510-T-C

175083706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968385-C-G

175083890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159968200-A-T

175083945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968145-A-G

175083961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968127-A-G

175083961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968127-A-T

175084107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968031-A-G

175084112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159968026-T-G

175084247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159967895-T-C

175084280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159967747-G-A

175084280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159967747-G-T

175084653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159967409-C-T

175085192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159967080-C-T

175085361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159966955-T-A

175085361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159966955-T-C

175085396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159966917-T-C

175085396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159966917-T-G

http://identifiers.org/hco/1/GRCh38#175085407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159966904-C-A

http://identifiers.org/hco/1/GRCh38#175085419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159966892-A-C

175085419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159966892-A-G

175085537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159966797-G-A

http://identifiers.org/hco/1/GRCh38#175085569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159966774-C-A

175085569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159966774-C-G

http://identifiers.org/hco/1/GRCh38#175085982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159966681-C-A

175085982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159966681-C-T

175086581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159966179-T-G

175086721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159966094-G-A

http://identifiers.org/hco/1/GRCh38#175086730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159966085-A-C

175087053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159965744-T-A

175087053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159965744-T-G

175088878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159964647-C-T

175088949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159964583-A-G

175089092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159964430-C-T

175090906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962835-T-C

175090924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962817-G-T

175091080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962659-G-A

175091080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962659-G-C

175091109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962630-C-T

175091252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962485-A-G

175091253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962484-G-A

175091267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962470-G-T

175091286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962457-A-G

http://identifiers.org/hco/1/GRCh38#175091374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159962376-A-C

175091434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962334-T-C

175091438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962330-T-C

175091639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962090-G-A

175091712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962027-C-T

175091735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159962005-T-C

175091994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159961127-G-A

175091994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159961127-G-C

175091994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159961127-G-T

175093391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159959138-G-A

175093524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159959014-G-A

http://identifiers.org/hco/1/GRCh38#175093551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159958981-C-A

175093551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159958981-C-T

175093801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159958681-A-G

175093852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159958631-A-G

175093951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159958548-G-T

175094103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159958402-G-C

175094133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159958372-C-T

175094256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159958249-A-G

175094734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159957016-C-T

175094881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159956873-A-G

175094915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159956839-C-T

175094947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159956817-A-G

http://identifiers.org/hco/1/GRCh38#175094973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159956791-C-A

175094973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159956791-C-T

http://identifiers.org/hco/1/GRCh38#175096601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159954905-C-A

175096601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159954905-C-T

175096675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159954834-T-C

175096708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159954803-A-G

175096714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159954797-T-A

175096807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159954721-G-A

175096948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159954586-C-T

175096999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159954535-T-G

175097134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159954413-T-C

175097200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159954372-C-G

http://identifiers.org/hco/1/GRCh38#175097402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159954178-A-C

175097402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159954178-A-G

175097406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159954174-C-G

175097406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159954174-C-T

175097476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, missense_variant
orthologous variants: 159954104-T-C

175097509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, missense_variant
orthologous variants: 159954071-T-C

175097582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, missense_variant
orthologous variants: 159954001-C-T

175097641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, missense_variant
orthologous variants: 159953942-G-A

175097703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159953880-C-G

175097736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159953847-A-G

175098227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159953278-C-G

175098227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159953278-C-T

175098297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159953218-C-T

175098309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159953206-C-G

175098382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, missense_variant
orthologous variants: 159953134-G-A

175098457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, missense_variant
orthologous variants: 159953059-A-G

http://identifiers.org/hco/1/GRCh38#175098484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159953032-C-A

175098614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952902-T-G

http://identifiers.org/hco/1/GRCh38#175098648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159952886-A-C

175098648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952886-A-G

175098659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952875-T-C

http://identifiers.org/hco/1/GRCh38#175098689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159952852-A-C

175098689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952852-A-T

175098701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952841-G-A

175098701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952841-G-T

175098715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952827-A-G

http://identifiers.org/hco/1/GRCh38#175098816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159952738-C-A

175098870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952676-G-C

175099071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952462-T-C

http://identifiers.org/hco/1/GRCh38#175099072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159952461-C-A

175099072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952461-C-T

175099096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952444-G-T

175099249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952298-G-A

175099255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952292-C-T

175099917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952172-G-A

175100078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159952062-C-G

175100172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159951964-G-C

175100366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159951779-A-G

175100380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159951765-A-T

175100390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159951755-T-C

175100427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159951723-G-A

http://identifiers.org/hco/1/GRCh38#175100480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159951676-A-C

175100593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159951560-A-G

175100593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159951560-A-T

http://identifiers.org/hco/1/GRCh38#175100649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159951504-A-C

175100668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159951485-T-C

175116153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159951293-G-C

175116337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159951099-T-C

175116552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159950894-C-T

175116631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159950811-A-G

175116710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159950719-G-T

175116729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159950687-G-T

175116805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159950613-A-G

175116817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159950602-A-G

175116891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159950533-T-C

175117232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159948039-T-C

http://identifiers.org/hco/1/GRCh38#175117298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159945816-C-A

http://identifiers.org/hco/1/GRCh38#175117332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159943511-C-A

175117332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159943511-C-T

http://identifiers.org/hco/1/GRCh38#175117338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159943505-A-C

175117338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159943505-A-G

175117429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159943241-T-G

175117509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159943143-G-C

http://identifiers.org/hco/1/GRCh38#175118436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159944015-A-C

175118552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159942333-T-C

175118566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, missense_variant
orthologous variants: 159942317-G-C

175118566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, missense_variant
orthologous variants: 159942317-G-T

175118674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, missense_variant
orthologous variants: 159942209-G-A

175118742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, missense_variant
orthologous variants: 159942141-G-T

175120100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159941212-G-A

175120370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159940939-G-A

175120656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159940663-G-A

175121371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159940305-T-A

175121493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159940184-G-C

175121514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159940168-T-C

175121526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159940157-A-G

175121979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159939724-T-A

175121979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159939724-T-C

175121980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159939723-A-G

http://identifiers.org/hco/1/GRCh38#175122761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159938997-A-C

http://identifiers.org/hco/1/GRCh38#175122997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159938791-C-A

175123076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159938736-C-T

175123255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159938559-A-G

175123291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159938183-T-C

175123426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159938051-A-G

175123453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159938024-A-T

175123522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159937955-G-A

175123622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159937855-G-A

175123732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159937763-G-A

175123732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159937763-G-T

175123797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159937697-T-C

175123946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159937227-T-G

http://identifiers.org/hco/1/GRCh38#175125289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159936190-A-C

175126523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159935134-T-C

175126676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159934974-C-T

175126863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159934789-T-C

175126863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159934789-T-G

175126871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159934782-G-A

175126871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159934782-G-T

http://identifiers.org/hco/1/GRCh38#175127026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159934638-C-A

175127026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159934638-C-G

175127026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159934638-C-T

175127111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159934554-C-T

175127544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159933547-C-T

175127715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159933387-C-T

175127720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159933382-A-G

175127947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159933185-G-A

175127947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159933185-G-T

http://identifiers.org/hco/1/GRCh38#175127969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159933158-C-A

175127973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159933154-G-C

http://identifiers.org/hco/1/GRCh38#175128014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159933115-C-A

http://identifiers.org/hco/1/GRCh38#175128136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159932994-C-A

175128136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: synonymous variant
orthologous variants: 159932994-C-T

175128230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932916-G-T

175128231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932915-G-C

175128231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932915-G-T

175128244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932902-A-G

175128258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932896-G-A

175128258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932896-G-T

175128263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932891-A-T

175128310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932860-A-G

http://identifiers.org/hco/1/GRCh38#175128316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159932854-A-C

175128316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932854-A-G

175128330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932840-G-A

175128383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932798-T-A

175128451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932688-A-T

175128456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932683-A-G

175128487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932649-G-A

175128557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932582-C-T

http://identifiers.org/hco/1/GRCh38#175128572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159932570-C-A

175128572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932570-C-T

http://identifiers.org/hco/1/GRCh38#175128573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159932569-A-C

175128573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932569-A-G

175128690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159932451-G-A

175128726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159932415-A-G

175128756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932384-G-A

175128777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932363-T-C

175128845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932303-T-A

175128845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932303-T-G

175129535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932160-T-C

175129628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159932082-G-A

175129920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159931785-G-A

175130023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159931686-T-A

http://identifiers.org/hco/1/GRCh38#175130144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159931567-C-A

http://identifiers.org/hco/1/GRCh38#175130220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#159931494-C-A

175130220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, undefined
orthologous variants: 159931494-C-T

175130297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, undefined
orthologous variants: 159931416-C-G

175130297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, undefined
orthologous variants: 159931416-C-T

175130482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159931220-C-G

175130517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159931189-G-A

175131139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159930308-C-G

175131861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159929634-T-C

175131861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159929634-T-G

175132070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159929422-T-C

175132241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159929258-C-G

175132462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159929016-G-A

175133158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159928350-A-G

175133266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159928234-C-T

175133469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159928048-C-T

175133691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159927857-T-A

175133778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159927781-C-T

175134854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159926883-G-A

175135090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159926654-A-G

175135392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159926382-A-G

175135785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925973-G-A

175135785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925973-G-T

175135836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925886-C-T

175135886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: synonymous variant
orthologous variants: 159925836-G-A

175135962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925759-A-G

175135976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925745-G-A

175136040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925680-A-G

175136041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925679-G-A

175136058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925662-G-A

175136058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925662-G-T

175136075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925647-A-T

175136086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925636-G-C

175136086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925636-G-T

175136164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925582-A-G

175136494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925261-A-G

http://identifiers.org/hco/1/GRCh38#175136691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159925056-C-A

http://identifiers.org/hco/1/GRCh38#175136719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159925028-A-C

175136719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925028-A-G

175136719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925028-A-T

http://identifiers.org/hco/1/GRCh38#175136720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159925027-C-A

175136720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159925027-C-G

http://identifiers.org/hco/1/GRCh38#175136773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159924977-C-A

175136773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159924977-C-T

http://identifiers.org/hco/1/GRCh38#175136775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159924975-C-A

175136775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159924975-C-T

http://identifiers.org/hco/1/GRCh38#175136779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159924971-C-A

175136780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159924970-A-G

175136780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159924970-A-T

175136985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense variant
orthologous variants: 159924765-G-A

175137540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159924234-G-T

175137691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159924091-T-G

175138189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159923685-C-T

175138376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159922923-G-A

175138376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159922923-G-T

175138616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159922739-A-G

175140091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159922110-C-T

175140145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159922058-A-T

175140197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159922006-G-A

http://identifiers.org/hco/1/GRCh38#175140478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159921748-C-A

175140565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159921664-G-A

175140675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159921554-G-A

175140764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159921464-T-A

175140764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159921464-T-C

175141067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159921178-C-G

http://identifiers.org/hco/1/GRCh38#175141126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159921039-C-A

175141126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159921039-C-T

175141231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159920942-A-G

175141327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159920866-T-C

175141346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159920847-A-G

175141346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159920847-A-T

175141367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159920826-A-G

175141396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159920792-A-G

http://identifiers.org/hco/1/GRCh38#175141413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159920775-A-C

175141459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159919705-G-A

175141512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159919657-C-T

175141513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159919656-T-C

http://identifiers.org/hco/1/GRCh38#175141584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159919588-C-A

175141618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159919554-G-A

175141871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159918579-T-C

175143028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159917360-A-G

175143109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159917280-C-G

175143109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159917280-C-T

175143336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159917092-G-C

175143829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916611-G-C

175143910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916527-T-C

175143932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916512-T-C

175143982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916474-T-C

175143982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916474-T-G

175144011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916444-G-A

175144018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916437-T-C

175144048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916409-T-G

175144053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916404-T-G

175144189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916313-T-C

175144244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916268-T-C

175144244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916268-T-G

175144352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159916171-C-G

http://identifiers.org/hco/1/GRCh38#175144613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159915899-C-A

175144613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159915899-C-T

175144771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159915754-G-A

175144830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159915716-C-T

175145770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159914852-G-A

175145770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159914852-G-T

175146589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, undefined
orthologous variants: 159914043-C-T

175146607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron variant
orthologous variants: 159914024-G-T

http://identifiers.org/hco/1/GRCh38#175146664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#159913971-C-A

175146664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, undefined
orthologous variants: 159913971-C-G

175146672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: intron_variant, undefined
orthologous variants: 159913964-C-G

175146997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: missense_variant, undefined
orthologous variants: 159913670-C-G

175147125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913550-G-A

175147125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913550-G-T

http://identifiers.org/hco/1/GRCh38#175147183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159913464-C-A

175147183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913464-C-T

http://identifiers.org/hco/1/GRCh38#175147189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159913458-A-C

175147198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913449-C-T

175147234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913413-T-C

175147380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913249-T-G

175147407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913218-T-C

http://identifiers.org/hco/1/GRCh38#175147449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159913183-C-A

175147449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913183-C-T

175147489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913142-G-A

175147489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913142-G-C

175147500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913131-G-C

175147521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913107-T-C

175147534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159913094-G-A

http://identifiers.org/hco/1/GRCh38#175147561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#159913067-C-A

175147823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159912814-G-A

175147852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159912760-A-G

175147875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22942
most severe consequence: 3 prime UTR variant
orthologous variants: 159912738-G-A