http://identifiers.org/hco/4/GRCh38#6575199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36987928-C-A

6575199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 5 prime UTR variant
orthologous variants: 36987928-C-T

6575230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36987898-T-C

6575253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36987875-T-A

6575253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: synonymous variant
orthologous variants: 36987875-T-C

6575432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36987732-G-A

6575432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36987732-G-T

6575458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36987700-T-A

6575481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36987676-T-A

6575481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36987676-T-C

6575647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36987502-C-T

6575656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36987494-G-A

6575656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36987494-G-C

http://identifiers.org/hco/4/GRCh38#6575763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36987382-C-A

http://identifiers.org/hco/4/GRCh38#6575881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36987249-C-A

6576587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36987107-C-G

6576587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36987107-C-T

6576623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36987071-G-A

http://identifiers.org/hco/4/GRCh38#6576635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36987059-C-A

6576635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36987059-C-T

6576756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36986931-C-G

6576756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36986931-C-T

http://identifiers.org/hco/4/GRCh38#6576762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36986925-C-A

http://identifiers.org/hco/4/GRCh38#6576785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36986894-A-C

http://identifiers.org/hco/4/GRCh38#6576788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36986891-C-A

6576973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36986751-C-T

6576979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36986745-G-T

6577246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36986536-C-G

6577288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36986495-G-A

6578065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36985614-A-T

6578066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36985613-G-A

6578123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36985555-T-C

6578281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36985399-G-A

6578281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36985399-G-T

6578362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36985342-G-A

6578456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36985248-G-A

6578456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36985248-G-C

http://identifiers.org/hco/4/GRCh38#6578489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36985215-C-A

6578523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36985107-A-T

http://identifiers.org/hco/4/GRCh38#6578600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36984843-A-C

6578600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36984843-A-T

6578841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36984588-A-G

6579066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36984359-C-T

6579135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36984290-C-G

6579135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36984290-C-T

6579138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36984287-C-T

6586723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36983781-G-A

6586858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36983678-G-T

6586866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36983671-G-A

6586866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36983671-G-C

6586866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36983671-G-T

http://identifiers.org/hco/4/GRCh38#6586882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36983661-C-A

6586882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36983661-C-T

http://identifiers.org/hco/4/GRCh38#6586921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36983623-C-A

6586921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36983623-C-G

6586921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36983623-C-T

6587049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36983501-C-G

6587127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36983423-C-T

http://identifiers.org/hco/4/GRCh38#6587210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36983347-C-A

6587210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36983347-C-T

6588940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36981655-G-A

6588940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36981655-G-T

6588954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36981641-G-A

6588954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36981641-G-T

http://identifiers.org/hco/4/GRCh38#6588956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36981639-A-C

6588958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36981637-G-A

6588975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36981621-G-A

6589063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36981531-C-G

6589063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: stop gained
orthologous variants: 36981531-C-T

6593162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36979367-C-T

http://identifiers.org/hco/4/GRCh38#6593166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36979363-C-A

6593166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 36979363-C-G

6593166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 36979363-C-T

http://identifiers.org/hco/4/GRCh38#6593223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36979306-A-C

6593246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36979283-G-A

6593257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: synonymous variant
orthologous variants: 36979272-C-G

6593257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: synonymous variant
orthologous variants: 36979272-C-T

6593315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, missense_variant
orthologous variants: 36979214-G-A

6593315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, missense_variant
orthologous variants: 36979214-G-T

6593327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, missense_variant
orthologous variants: 36979202-A-G

6593403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36979121-G-A

6593403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36979121-G-T

6593417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36979109-C-G

6593417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36979109-C-T

6593601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978939-G-A

6593804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978796-T-C

6593849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978766-G-T

http://identifiers.org/hco/4/GRCh38#6594397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36978534-A-C

6594397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978534-A-G

6594483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978475-G-A

6594483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978475-G-T

6594495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978463-G-T

6594510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978444-G-T

6594511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978443-A-T

6594582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, missense_variant
orthologous variants: 36978374-G-A

6594582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, missense_variant
orthologous variants: 36978374-G-T

6594648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36978308-C-G

6594651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36978305-G-A

6594651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36978305-G-T

6594707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: synonymous variant
orthologous variants: 36978249-C-T

6594742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978214-T-A

6594743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978213-C-T

http://identifiers.org/hco/4/GRCh38#6594760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36978198-A-C

6594769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978190-G-A

6594769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978190-G-T

6594813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978156-T-A

6594813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978156-T-C

6594819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978150-G-A

6594819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978150-G-T

http://identifiers.org/hco/4/GRCh38#6594852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36978132-C-A

6594852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978132-C-T

6595026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36978044-C-T

6595204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36977870-G-A

6595514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36977586-A-G

http://identifiers.org/hco/4/GRCh38#6595548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36977556-C-A

6595643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36977475-A-G

6596191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, undefined
orthologous variants: 36976862-C-G

6596196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, undefined
orthologous variants: 36976857-T-G

6596273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976767-G-A

6596514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976553-C-G

6596529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976543-T-C

6596535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976537-C-T

6596605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976483-T-G

6596704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976378-C-G

6596704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976378-C-T

http://identifiers.org/hco/4/GRCh38#6596772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36976304-C-A

6596835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976235-C-T

6596921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976149-A-T

6596965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976122-G-T

http://identifiers.org/hco/4/GRCh38#6596968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36976119-C-A

6596968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976119-C-G

6596968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976119-C-T

6597049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976053-G-A

6597049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36976053-G-C

6597348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36975761-G-C

6597348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36975761-G-T

6597369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36975744-G-T

http://identifiers.org/hco/4/GRCh38#6597376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36975737-C-A

http://identifiers.org/hco/4/GRCh38#6597426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36975729-A-C

6597426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36975729-A-G

6597495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36975655-T-C

http://identifiers.org/hco/4/GRCh38#6597628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36975535-A-C

6597800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36975421-T-C

http://identifiers.org/hco/4/GRCh38#6597986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36975199-C-A

6598362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 36974889-G-T

6598364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36974887-G-A

6598485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36974624-G-A

6598485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36974624-G-T

6598560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36974548-T-C

6598636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36974483-G-T

6599810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36974025-T-A

6600469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36973660-C-G

http://identifiers.org/hco/4/GRCh38#6600488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36973648-C-A

http://identifiers.org/hco/4/GRCh38#6600495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36973641-C-A

6600495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36973641-C-G

6600495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36973641-C-T

6600527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36973609-T-C

http://identifiers.org/hco/4/GRCh38#6600742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36973415-C-A

http://identifiers.org/hco/4/GRCh38#6600749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36973408-C-A

6600749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36973408-C-T

6600762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36973395-G-T

6605070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36972920-G-C

6605112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36972878-C-G

6605112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36972878-C-T

6605150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: synonymous variant
orthologous variants: 36972840-T-C

6605178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36972812-C-T

6605296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36972694-A-G

6605297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36972693-G-A

6605340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36972650-G-A

6605349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36972641-G-A

6605349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36972641-G-T

http://identifiers.org/hco/4/GRCh38#6605382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36972612-C-A

6605382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36972612-C-G

http://identifiers.org/hco/4/GRCh38#6605418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36972577-C-A

6605418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36972577-C-G

6605420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36972575-T-G

6605543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36972461-G-T

6605554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36972450-A-G

6605600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36972405-T-C

6609160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36971809-A-G

6609160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36971809-A-T

6609237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36971732-G-A

6609237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36971732-G-C

6609354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36971655-G-A

6609354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36971655-G-C

http://identifiers.org/hco/4/GRCh38#6609386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36971630-C-A

6609386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36971630-C-G

6609388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36971628-G-T

6609402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36971608-G-A

6609402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36971608-G-C

6609402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36971608-G-T

6609425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36971577-G-A

6609425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36971577-G-T

6609440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36971558-T-A

6609475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36971523-T-G

6609481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36971519-G-A

6609481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36971519-G-T

6609499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36971502-T-C

http://identifiers.org/hco/4/GRCh38#6609698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36971386-C-A

6609698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36971386-C-G

6609698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36971386-C-T

6609729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36971366-A-G

http://identifiers.org/hco/4/GRCh38#6609796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36971322-A-C

6609862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36971262-C-T

6609952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36971172-A-G

6610109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36971018-A-T

6610146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970989-C-G

6610779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970795-C-T

6610790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970784-G-A

6610790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970784-G-C

http://identifiers.org/hco/4/GRCh38#6610851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36970748-C-A

6610851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970748-C-T

6610955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36970646-C-G

6611009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970583-C-G

6611010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970582-C-G

6611015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970577-G-A

6611060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970523-G-A

6611060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970523-G-T

http://identifiers.org/hco/4/GRCh38#6611170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36970418-C-A

http://identifiers.org/hco/4/GRCh38#6611227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36970361-A-C

6611227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense variant
orthologous variants: 36970361-A-G

6611284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970304-G-A

6611284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970304-G-C

6611286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 36970302-G-A

http://identifiers.org/hco/4/GRCh38#6611310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36970277-C-A

6611310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970277-C-G

http://identifiers.org/hco/4/GRCh38#6611355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36970243-C-A

6611355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970243-C-T

http://identifiers.org/hco/4/GRCh38#6611406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36970201-C-A

6611406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970201-C-T

6611522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36970111-T-C

6614075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36967869-G-A

6614075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36967869-G-T

6614095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36967857-A-G

http://identifiers.org/hco/4/GRCh38#6614120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36967834-C-A

6614120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36967834-C-G

6614120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36967834-C-T

6614146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36967812-G-A

6614146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36967812-G-T

6614207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36967761-C-T

6614504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36967533-A-G

6617266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36966547-G-A

6617266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36966547-G-C

6617266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36966547-G-T

6617274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36966539-T-C

6617274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36966539-T-G

http://identifiers.org/hco/4/GRCh38#6617286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36966527-A-C

6617287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36966526-T-A

6617287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36966526-T-G

6617294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: 36966519-G-T

http://identifiers.org/hco/4/GRCh38#6617359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36966474-A-C

6617385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: stop gained
orthologous variants: 36966453-C-T

6617468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36966370-T-C

6617475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36966363-G-A

6619656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36965504-G-A

6619656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36965504-G-T

http://identifiers.org/hco/4/GRCh38#6619692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36965463-C-A

6619692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36965463-C-G

6619929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, splice_region_variant, synonymous_variant
orthologous variants: 36965243-T-C

http://identifiers.org/hco/4/GRCh38#6619959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36965213-A-C

6619995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 36965177-G-A

6619995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 36965177-G-T

6620103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36965087-G-A

6620103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36965087-G-T

http://identifiers.org/hco/4/GRCh38#6620110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36965080-C-A

http://identifiers.org/hco/4/GRCh38#6620192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36965021-C-A

6620192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36965021-C-T

6620224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36964991-G-C

6620224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36964991-G-T

6620265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36964949-G-C

6620265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36964949-G-T

6620906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36964732-T-A

6620906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36964732-T-C

6620906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36964732-T-G

6620908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36964730-T-A

6620908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36964730-T-C

6620908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36964730-T-G

6621106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36964627-T-C

6621304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3 prime UTR variant
orthologous variants: 36964445-G-A

http://identifiers.org/hco/4/GRCh38#6621309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36964440-C-A

6621442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3 prime UTR variant
orthologous variants: 36964302-C-G

6621442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3 prime UTR variant
orthologous variants: 36964302-C-T

http://identifiers.org/hco/4/GRCh38#6621519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29623
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36964236-C-A