117900703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258817-T-C

117900703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258817-T-G

http://identifiers.org/hco/11/GRCh38#117900707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45258809-C-A

117900707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258809-C-T

117900740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258777-A-G

117900893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258659-C-T

117900920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258631-G-T

http://identifiers.org/hco/11/GRCh38#117900926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45258626-C-A

117900926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258626-C-T

117900937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258615-G-A

http://identifiers.org/hco/11/GRCh38#117900943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45258609-C-A

117900943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258609-C-T

117901160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258460-T-C

117901224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258396-C-T

117901287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258328-T-C

117901287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258328-T-G

117901436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258193-C-T

117901469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258140-T-G

http://identifiers.org/hco/11/GRCh38#117901481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45258128-C-A

http://identifiers.org/hco/11/GRCh38#117901498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45258111-C-A

117901511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258074-G-A

117901511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258074-G-T

117901538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258047-G-A

117901538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258047-G-C

117901538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45258047-G-T

117901751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257846-T-C

117901751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257846-T-G

117901763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257830-C-T

117901764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257829-G-A

117901764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257829-G-C

117901764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257829-G-T

117901766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257827-T-C

117901766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257827-T-G

http://identifiers.org/hco/11/GRCh38#117901767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45257826-C-A

117901770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257823-G-T

117901783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257809-T-C

117901899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257682-G-T

117902002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257586-G-A

117902002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257586-G-C

http://identifiers.org/hco/11/GRCh38#117902058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45257532-C-A

117902058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257532-C-T

117902137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3 prime UTR variant
orthologous variants: 45257405-G-T

117902348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45257218-T-A

117902350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45257216-T-A

117902350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45257216-T-C

http://identifiers.org/hco/11/GRCh38#117902401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45257162-A-C

117902401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45257162-A-G

117902491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45257101-C-T

117902516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45257078-C-T

http://identifiers.org/hco/11/GRCh38#117902524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45257071-C-A

117903445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 45256848-C-T

117903446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 45256847-T-A

117903446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 45256847-T-G

117903447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 45256846-G-A

117903447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant, stop_gained
orthologous variants: 45256846-G-C

http://identifiers.org/hco/11/GRCh38#117903504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45256790-C-A

117903504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45256790-C-G

117903504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45256790-C-T

http://identifiers.org/hco/11/GRCh38#117903587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45256707-C-A

117903587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron_variant, missense_variant
orthologous variants: 45256707-C-T

http://identifiers.org/hco/11/GRCh38#117903891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45256419-C-A

http://identifiers.org/hco/11/GRCh38#117903911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45256399-C-A

117903911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45256399-C-T

117903913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45256397-A-G

117904222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45256093-G-T

117904227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45256088-G-A

117904227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45256088-G-T

117904237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45256078-G-A

117904360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45255995-C-T

117905474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45254739-G-A

117905528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45254694-A-G

117905528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45254694-A-T

http://identifiers.org/hco/11/GRCh38#117905618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45254608-C-A

117905618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45254608-C-G

http://identifiers.org/hco/11/GRCh38#117905703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45254491-C-A

117905709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: missense variant
orthologous variants: 45254485-A-G

117905778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45254421-A-G

117905798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45254403-G-A

117905798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45254403-G-C

117905798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45254403-G-T

117906016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45254274-G-A

117906135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45254264-C-T

117906199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45254246-G-A

117906321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45254135-A-G

117906891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45253165-A-G

117906934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45253121-G-A

117907147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45253016-A-G

http://identifiers.org/hco/11/GRCh38#117907274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45252888-A-C

http://identifiers.org/hco/11/GRCh38#117907324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45252872-C-A

117907324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45252872-C-T

117907343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45252853-G-A

117907343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45252853-G-C

117907343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45252853-G-T

117907349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45252847-G-A

117907349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45252847-G-T

117907366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45252830-C-G

117907366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45252830-C-T

117907492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252706-A-G

117907547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252653-A-T

117907559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252641-A-G

117907617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252575-G-C

117907617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252575-G-T

117907691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252330-T-C

117907692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252329-C-T

117907725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252281-G-T

117907767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252235-C-T

117907783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252221-T-A

117907806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252199-T-G

117907881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252121-A-G

117907968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252044-G-A

117907968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252044-G-T

http://identifiers.org/hco/11/GRCh38#117907978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45252034-C-A

117907986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45252026-A-G

http://identifiers.org/hco/11/GRCh38#117908007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45252004-A-C

117908012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251999-G-A

117908012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251999-G-T

117908032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251988-G-A

117908037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251983-T-C

http://identifiers.org/hco/11/GRCh38#117908078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45251942-C-A

117908078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251942-C-G

117908078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251942-C-T

117908110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251911-T-A

117908110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251911-T-C

117908110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251911-T-G

117908111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251910-G-T

117908113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251908-G-A

117908113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251908-G-C

117908113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251908-G-T

117908215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251814-A-G

117908220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251812-A-G

117908266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251766-T-C

http://identifiers.org/hco/11/GRCh38#117908287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45251745-C-A

117908287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45251745-C-T

117908512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron_variant, missense_variant
orthologous variants: 45250773-T-C

117908512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron_variant, missense_variant
orthologous variants: 45250773-T-G

117908764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: missense variant
orthologous variants: 45250551-T-C

http://identifiers.org/hco/11/GRCh38#117908845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45250472-C-A

http://identifiers.org/hco/11/GRCh38#117908855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45250462-C-A

117908859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45250444-G-T

117908893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45250410-G-A

117908893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45250410-G-T

117908946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45250362-A-G

117909045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45250265-C-T

117909054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45250258-A-G

117909522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45249959-C-T

117909523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45249958-T-C

117909533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45249948-G-C

117909674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45249828-G-T

117909690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45249812-G-A

117909690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45249812-G-T

117909693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45249809-G-T

http://identifiers.org/hco/11/GRCh38#117909790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#45249730-C-A

117909809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: missense_variant, undefined
orthologous variants: 45249711-A-G

117909824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: missense_variant, undefined
orthologous variants: 45249696-G-A

117909824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: missense_variant, undefined
orthologous variants: 45249696-G-T

117909917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: missense_variant, undefined
orthologous variants: 45249603-G-A

http://identifiers.org/hco/11/GRCh38#117909925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45249595-C-A

117909925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: synonymous variant
orthologous variants: 45249595-C-T

http://identifiers.org/hco/11/GRCh38#117910056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#45249488-C-A

117910056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron_variant, undefined
orthologous variants: 45249488-C-T

117910062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron_variant, undefined
orthologous variants: 45249481-C-T

117910200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45249370-G-A

117910320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45249087-G-C

117910550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45248747-G-T

117910566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45248722-A-G

http://identifiers.org/hco/11/GRCh38#117910568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45248720-C-A

117910568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: intron variant
orthologous variants: 45248720-C-G

117910587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45248673-G-A

117910587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45248673-G-T

http://identifiers.org/hco/11/GRCh38#117910601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45248659-C-A

117910601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45248659-C-T

http://identifiers.org/hco/11/GRCh38#117910687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45248405-C-A

117910752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, undefined
orthologous variants: 45248340-T-A

117910752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, undefined
orthologous variants: 45248340-T-C

117910827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45248274-G-T

117910874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45248232-G-T

117911126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247985-A-G

http://identifiers.org/hco/11/GRCh38#117911480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45247738-C-A

117911480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247738-C-T

117911689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247558-G-A

117911689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247558-G-T

http://identifiers.org/hco/11/GRCh38#117911695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45247552-C-A

117911695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247552-C-T

http://identifiers.org/hco/11/GRCh38#117911709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45247537-C-A

117911709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247537-C-T

http://identifiers.org/hco/11/GRCh38#117911712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45247534-C-A

117911712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247534-C-G

117911753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247493-C-T

117911759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247491-C-T

http://identifiers.org/hco/11/GRCh38#117911768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45247482-C-A

117911896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247360-T-C

117911897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247359-G-A

117911897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247359-G-T

http://identifiers.org/hco/11/GRCh38#117911912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45247345-C-A

http://identifiers.org/hco/11/GRCh38#117911922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45247335-C-A

117911922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247335-C-T

117911943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247314-G-A

117911943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247314-G-T

http://identifiers.org/hco/11/GRCh38#117911960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45247298-C-A

117911960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247298-C-G

117911971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247287-G-A

117911971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247287-G-T

117912141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45247153-C-T

http://identifiers.org/hco/11/GRCh38#117912425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45246505-C-A

117912425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45246505-C-T

117912476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45246455-T-A

117912542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45246390-C-G

117913083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45245884-A-G

http://identifiers.org/hco/11/GRCh38#117913115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45245782-C-A

http://identifiers.org/hco/11/GRCh38#117913116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45245781-A-C

117913153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45245665-A-T

117913215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45245485-T-C

117913260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45245428-G-A

117913407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45245291-A-G

117913506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45245245-G-A

http://identifiers.org/hco/11/GRCh38#117913725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45245029-A-C

117913952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45244804-G-T

117913994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45244763-A-G

117914229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45244043-A-G

117914259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45244019-A-G

117914302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243976-C-T

117914305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243973-G-A

117914305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243973-G-T

117914352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243925-C-T

117914362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243915-C-T

117914374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243903-C-G

117914374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243903-C-T

117914375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243902-G-A

117914375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243902-G-T

117914585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243680-A-G

117914585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243680-A-T

117914655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243610-G-C

117914740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243534-C-G

117914812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243462-C-T

117914840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243433-G-T

117915167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243097-G-A

117915167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243097-G-C

117915182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45243086-A-G

117915311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242973-T-G

117915322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242962-C-T

117915397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242887-G-A

117915404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242881-G-A

117915790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242539-G-T

117915837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242493-G-A

117915871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242465-G-A

117915916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242420-A-T

117915964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242380-C-T

117915985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242363-G-A

117915985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242363-G-C

117916154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242186-T-C

117916203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45242154-C-T

http://identifiers.org/hco/11/GRCh38#117916342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45242029-C-A

117916501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241896-G-A

117916839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241558-T-C

117916992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241404-C-G

117916992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241404-C-T

http://identifiers.org/hco/11/GRCh38#117917018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45241378-C-A

117917018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241378-C-T

117917038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241373-G-A

117917038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241373-G-T

http://identifiers.org/hco/11/GRCh38#117917042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45241369-C-A

117917042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241369-C-T

117917111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241322-G-A

117917111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241322-G-T

117917120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241314-T-A

117917120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241314-T-C

http://identifiers.org/hco/11/GRCh38#117917121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45241313-C-A

117917121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241313-C-T

http://identifiers.org/hco/11/GRCh38#117917127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45241307-A-C

117917128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241306-G-A

117917128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241306-G-C

117917128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241306-G-T

http://identifiers.org/hco/11/GRCh38#117917134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45241300-C-A

117917134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45241300-C-T

117917272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 45241163-T-C

117917280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45241155-A-G

117917286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45241149-G-T

http://identifiers.org/hco/11/GRCh38#117917385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45241071-C-A

117917537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240958-C-G

http://identifiers.org/hco/11/GRCh38#117917564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45240929-C-A

117917564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240929-C-T

117917937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240557-C-T

117918198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240288-C-G

117918198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240288-C-T

http://identifiers.org/hco/11/GRCh38#117918262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45240224-C-A

117918262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240224-C-T

http://identifiers.org/hco/11/GRCh38#117918276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45240210-C-A

117918276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240210-C-T

http://identifiers.org/hco/11/GRCh38#117918302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45240189-C-A

117918302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240189-C-G

117918302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240189-C-T

http://identifiers.org/hco/11/GRCh38#117918319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45240168-A-C

117918319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240168-A-G

117918319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240168-A-T

117918341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240149-C-G

117918363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240128-G-A

117918363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240128-G-T

117918366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45240125-C-T

117918596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45239898-C-G

117918603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45239891-G-A

117918653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45239841-T-C

117918713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45239802-T-G

117918728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45239787-T-C

117918758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45239775-T-C

117918812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45239739-T-C

117919573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45238606-C-T

http://identifiers.org/hco/11/GRCh38#117919598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45238581-C-A

117919733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45238472-T-C

http://identifiers.org/hco/11/GRCh38#117919865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45238364-C-A

http://identifiers.org/hco/11/GRCh38#117919903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45238335-C-A

117920013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45238225-T-A

117920079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45238147-G-A

http://identifiers.org/hco/11/GRCh38#117921031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45237741-A-C

http://identifiers.org/hco/11/GRCh38#117921144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45237461-C-A

117921144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45237461-C-T

117921256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45237362-T-C

http://identifiers.org/hco/11/GRCh38#117921273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45237352-A-C

117921591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45237030-G-A

117921591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45237030-G-T

http://identifiers.org/hco/11/GRCh38#117921626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45236996-C-A

117921626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45236996-C-T

117921849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45236776-C-G

http://identifiers.org/hco/11/GRCh38#117921993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45236652-C-A

117922159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45236487-C-G

117922159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45236487-C-T

117923073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45235918-G-A

117923244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45235651-G-A

117923275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45235609-C-T

117923278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45235606-C-G

117923335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45235575-G-A

http://identifiers.org/hco/11/GRCh38#117923369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45235540-C-A

117924235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45235247-G-A

117924235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45235247-G-T

117924244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45235238-G-A

117924282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45235208-G-C

117924462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45235061-G-A

117924815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45234659-C-T

117924825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45234649-G-A

117924825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45234649-G-T

117924842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45234630-T-C

117924889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45234580-A-G

117925001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45234518-C-T

http://identifiers.org/hco/11/GRCh38#117925002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45234517-C-A

117925002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45234517-C-T

http://identifiers.org/hco/11/GRCh38#117925267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45234252-C-A

117925267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45234252-C-T

117925281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45234238-A-G

117926444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45233111-C-T

117926673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45232904-G-A

117926832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45232773-G-A

http://identifiers.org/hco/11/GRCh38#117926892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45232728-C-A

http://identifiers.org/hco/11/GRCh38#117926918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45232702-C-A

117927910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45231666-T-C

117927933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45231658-G-T

117928007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45231585-C-T

117928423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45231243-T-C

117928495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45231172-T-C

117928546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45231121-G-A

117928946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45230780-T-A

117928946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45230780-T-G

117929144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45230582-G-A

117929144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45230582-G-T

117929169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45230559-C-T

http://identifiers.org/hco/11/GRCh38#117929190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45230538-C-A

117929190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45230538-C-G

117929190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45230538-C-T

117929206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45230520-G-A

117929206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45230520-G-T

117929277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45230461-T-C

117929323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 45230417-G-C

117929323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 45230417-G-T

117929366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45230374-G-T

http://identifiers.org/hco/11/GRCh38#117929421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45230320-C-A

117929421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 45230320-C-T

http://identifiers.org/hco/11/GRCh38#117929427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#45230314-C-A

117929427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 45230314-C-G

117929427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29808
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 45230314-C-T