72837009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100933333-T-C

72837069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100933276-T-C

72837529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100932883-A-G

72837612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100932843-G-A

72837612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100932843-G-T

72837686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100932778-C-T

72837690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100932774-A-G

http://identifiers.org/hco/11/GRCh38#72837747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100932720-C-A

72837747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100932720-C-T

72837767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100932700-T-G

72837781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100932687-A-G

72837957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100932511-G-T

72838181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100932296-G-T

72838574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100931923-T-G

72838666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100931861-C-T

72838801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron_variant, missense_variant
orthologous variants: 100931728-G-A

72838801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron_variant, missense_variant
orthologous variants: 100931728-G-T

72838901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100931629-G-A

72838901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100931629-G-T

72838910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100931623-T-C

72838910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100931623-T-G

72838963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100931574-G-T

http://identifiers.org/hco/11/GRCh38#72838984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100931555-C-A

72838984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100931555-C-T

72839442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100931066-G-C

72839723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100930714-T-C

72839816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100930638-A-G

72839832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100930622-T-C

72840197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100930240-C-T

72840841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100927895-T-C

72841525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 100927614-G-A

72842355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100927023-T-C

72842983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100926354-G-T

http://identifiers.org/hco/11/GRCh38#72843016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100926321-C-A

72843016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100926321-C-T

72843227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, synonymous_variant
orthologous variants: 100926132-C-T

72843702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100925665-T-A

72843702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100925665-T-C

72844341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100925316-G-T

72844776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100924956-C-T

72844934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100924606-T-C

72844983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100924523-T-C

72845030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100924467-G-C

72845814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100923844-G-C

72849599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100921056-C-G

72850247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100920485-T-C

72850371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100920342-A-G

72850785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100919164-G-C

72857305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100917063-C-T

72858113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100916604-G-A

http://identifiers.org/hco/11/GRCh38#72864793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100911910-A-C

72865151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 100911383-G-A

72866987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100909873-T-C

72867011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100909848-C-G

http://identifiers.org/hco/11/GRCh38#72867616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100909214-A-C

72869669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100908528-G-C

72874602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100907175-G-A

72885726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100904458-G-C

72887360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100902949-G-C

72887360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100902949-G-T

72887394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100902914-G-A

72887394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100902914-G-T

72887561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 100902748-A-G

72887561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 100902748-A-T

72887606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100902718-T-C

72889952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 100899643-T-A

72889952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 100899643-T-C

72889953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 100899642-A-G

72898547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100898944-C-G

72899780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100896044-T-A

72899788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100896036-G-T

72900027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100895813-T-C

http://identifiers.org/hco/11/GRCh38#72900235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100895595-C-A

72900235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100895595-C-T

72900239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100895591-G-A

72900239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100895591-G-C

72900239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100895591-G-T

http://identifiers.org/hco/11/GRCh38#72900248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100895587-C-A

72900248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100895587-C-T

72900436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100895398-A-G

72900485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100895349-T-C

72900536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100895298-T-C

72900800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100894742-C-T

72902394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100893532-A-T

72902445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100893483-T-C

http://identifiers.org/hco/11/GRCh38#72902495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100893455-C-A

72902723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100892608-T-C

72902756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100892573-T-A

72902756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100892573-T-C

72902799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100892530-G-T

72918196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100887406-C-G

72920195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100885116-T-A

72920354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100884967-T-A

72920499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100884740-G-C

http://identifiers.org/hco/11/GRCh38#72920500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100884739-A-C

72921056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100884025-G-C

72921691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100883319-G-A

72921691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100883319-G-T

72921990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100883037-A-T

72922078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100882956-T-C

72924819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100880627-T-C

72932381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100879884-A-G

72932469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100879798-T-A

72932469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100879798-T-C

72932878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100879409-C-T

72934915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100877882-A-G

72934915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100877882-A-T

72935220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100877570-A-T

72935421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100877369-C-T

72935633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100877151-C-G

72935959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100876852-T-C

72936040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100876802-T-C

72936054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100876789-C-G

72936054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100876789-C-T

72936277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100876603-G-C

72936390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100876500-A-G

72937923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100871127-G-A

72940256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100870683-T-C

72941268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100870267-C-T

72950648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100865075-T-C

72951303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100864462-G-A

72951694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100863726-G-C

72952574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100862800-C-T

72952671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100862724-T-C

72952959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100862326-A-G

72953342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100861948-T-C

72953529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100861013-T-C

72953558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100860986-C-G

http://identifiers.org/hco/11/GRCh38#72960906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100860481-A-C

72961130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100860271-T-A

72961319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100860208-G-C

72961932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100859827-G-A

72962248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100859529-G-A

72962288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron_variant, undefined
orthologous variants: 100859344-T-C

72974662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100853897-T-A

72974983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100853539-A-G

http://identifiers.org/hco/11/GRCh38#72975798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100853080-C-A

72976244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100852613-G-A

72981488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100849783-G-A

72981974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100849564-C-G

72981974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100849564-C-T

72982987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100848584-T-C

72983048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100848542-A-T

72983688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100848238-G-A

72983688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100848238-G-T

72983713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100848213-C-T

72983718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100848208-A-G

72983761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100848167-G-T

72983838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100848081-A-G

72983973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100847903-T-C

72984235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100847667-A-T

72984317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100847446-G-A

72984317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100847446-G-C

72984364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100847407-T-A

72984939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100846256-G-A

72984939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100846256-G-T

http://identifiers.org/hco/11/GRCh38#72984999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100846196-C-A

72984999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100846196-C-T

72985035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100846165-T-C

72985257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100845949-G-A

72985257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100845949-G-T

72985614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100845854-T-C

72985669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100845801-G-A

72985729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100845745-G-C

72985791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100845679-G-A

72985905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100845562-C-T

72986102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100845379-G-C

72986592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100845060-C-G

72986592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100845060-C-T

http://identifiers.org/hco/11/GRCh38#72987115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100843987-A-C

72987115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100843987-A-G

72987288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100843825-A-G

72987725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100843354-G-A

72987875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100843018-G-C

http://identifiers.org/hco/11/GRCh38#72988820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100841148-C-A

72988820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100841148-C-T

http://identifiers.org/hco/11/GRCh38#72988837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100841131-A-C

http://identifiers.org/hco/11/GRCh38#72988854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100841114-C-A

72989416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100840578-T-C

72999849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100837739-C-G

73000164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100837436-T-A

73000592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100836438-C-T

73000860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100835869-T-A

73000908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100835811-T-C

73000908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100835811-T-G

73001559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100835335-A-G

73001569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100835325-G-A

73001665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100835255-G-A

73001665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100835255-G-C

73001684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100835242-G-A

73001684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100835242-G-C

73001751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100835193-T-C

73002511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100834455-G-A

73002532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100834439-G-A

73002929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100834214-G-A

73008460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100830680-G-A

http://identifiers.org/hco/11/GRCh38#73008697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100830461-A-C

73008876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100830266-T-C

73012961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100828015-G-A

73012961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100828015-G-C

73013090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100827907-C-T

http://identifiers.org/hco/11/GRCh38#73013187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100827816-A-C

73013313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100827686-C-G

73013500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100827517-A-G

73015666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100826866-T-C

http://identifiers.org/hco/11/GRCh38#73017477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100825723-A-C

http://identifiers.org/hco/11/GRCh38#73017663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100825439-A-C

73018482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100824688-T-C

73018661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100824518-T-C

73019214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100824019-G-A

73020284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100822715-A-G

73020594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100822429-T-C

73033894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100818825-A-G

73034529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100818186-C-T

73036252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100814914-T-C

73039915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100810006-T-C

http://identifiers.org/hco/11/GRCh38#73040017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100809902-A-C

73040196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100809727-C-T

73049213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100805570-T-C

73049421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100805775-G-A

73049421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100805775-G-C

73057118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100795504-A-G

73071933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100793388-G-A

73072119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100793212-G-C

73072251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100793082-G-A

73072736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100792671-C-G

73073334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100791980-C-T

73073806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100790891-A-T

73073852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100790847-G-T

http://identifiers.org/hco/11/GRCh38#73083628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100788462-A-C

73083654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100788443-A-G

http://identifiers.org/hco/11/GRCh38#73083706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: http://identifiers.org/mco/7/GRCm39#100788390-C-A

73083706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 100788390-C-G

73083706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 100788390-C-T

73083784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100788312-T-A

73083790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100788306-A-G

73083855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100788240-T-C

73088800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100786427-T-G

73088815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100786412-T-C

73095718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100780769-A-T

73095765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100780726-A-G

73103959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100778202-T-C

73104053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100778130-C-T

73104114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100778069-T-G

73104220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100777961-T-C

73127574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100773589-C-T

http://identifiers.org/hco/11/GRCh38#73128045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100773285-C-A

73128126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100773243-G-A

73128126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100773243-G-C

73128801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100772384-C-G

73130529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100771843-C-T

73135622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100768865-C-T

73135768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100768719-T-A

73135884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100768611-G-A

73137231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100765603-G-A

73137705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100764040-G-C

73138382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100763272-G-A

73138508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100763158-T-C

73139960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100760109-G-T

73140162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100759910-T-C

73140162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100759910-T-G

http://identifiers.org/hco/11/GRCh38#73140250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100759820-C-A

73140490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100759644-C-G

73140982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100759171-G-A

73141136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100759019-G-A

73141136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100759019-G-T

73141165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100758994-T-C

73141217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100758942-G-A

73141217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100758942-G-C

73141217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100758942-G-T

http://identifiers.org/hco/11/GRCh38#73141218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100758941-C-A

73141218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100758941-C-T

73141335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100758802-G-A

73141335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100758802-G-T

73141420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 100758713-A-G

73141725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100758385-A-G

73141815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron_variant, undefined
orthologous variants: 100758295-C-G

73141815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron_variant, undefined
orthologous variants: 100758295-C-T

73141826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100758279-G-A

73141826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: intron variant
orthologous variants: 100758279-G-T

http://identifiers.org/hco/11/GRCh38#73141902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#100758191-C-A

73141907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5 prime UTR variant
orthologous variants: 100758186-C-T

73141997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5 prime UTR variant
orthologous variants: 100758085-A-T

73142104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5 prime UTR variant
orthologous variants: 100757973-C-G

73142193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5 prime UTR variant
orthologous variants: 100757896-T-A

73142193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5 prime UTR variant
orthologous variants: 100757896-T-C

73142193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5 prime UTR variant
orthologous variants: 100757896-T-G

http://identifiers.org/hco/11/GRCh38#73142194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100757895-C-A

http://identifiers.org/hco/11/GRCh38#73142201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#100757888-C-A

73142201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5 prime UTR variant
orthologous variants: 100757888-C-T

73142278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5 prime UTR variant
orthologous variants: 100757812-G-A

73142278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29114
most severe consequence: 5 prime UTR variant
orthologous variants: 100757812-G-T