34551448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3 prime UTR variant
orthologous variants: 41657515-G-A

34551448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3 prime UTR variant
orthologous variants: 41657515-G-C

34551448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3 prime UTR variant
orthologous variants: 41657515-G-T

http://identifiers.org/hco/9/GRCh38#34551591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41657658-A-C

34551591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3 prime UTR variant
orthologous variants: 41657658-A-G

34551591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3 prime UTR variant
orthologous variants: 41657658-A-T

http://identifiers.org/hco/9/GRCh38#34551599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41657666-C-A

34551708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3 prime UTR variant
orthologous variants: 41657776-G-T

http://identifiers.org/hco/9/GRCh38#34551912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41657992-C-A

34551912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3 prime UTR variant
orthologous variants: 41657992-C-T

34552042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3 prime UTR variant
orthologous variants: 41658122-G-A

34552042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3 prime UTR variant
orthologous variants: 41658122-G-T

http://identifiers.org/hco/9/GRCh38#34552133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41658216-C-A

34552133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41658216-C-T

34552193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 41658273-G-A

34552193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 41658273-G-T

http://identifiers.org/hco/9/GRCh38#34552224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41658304-A-C

34552224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 41658304-A-T

34552233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 41658313-G-A

http://identifiers.org/hco/9/GRCh38#34552374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41658454-C-A

34552374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41658454-C-G

34552466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41658528-G-C

34552466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41658528-G-T

34552540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41658600-G-T

http://identifiers.org/hco/9/GRCh38#34552546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41658606-C-A

34552546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41658606-C-T

http://identifiers.org/hco/9/GRCh38#34552594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41658691-C-A

34552594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41658691-C-T

34552675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 41658782-C-T

34552679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: missense variant
orthologous variants: 41658786-G-A

34552679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: missense variant
orthologous variants: 41658786-G-T

34552690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: synonymous variant
orthologous variants: 41658797-C-G

34552690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: synonymous variant
orthologous variants: 41658797-C-T

34552831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: synonymous variant
orthologous variants: 41658938-T-A

34552831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: synonymous variant
orthologous variants: 41658938-T-C

34552843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: synonymous variant
orthologous variants: 41658950-G-A

34552843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: synonymous variant
orthologous variants: 41658950-G-T

34552979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41659072-T-C

34553241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41659268-G-A

34553623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41659566-G-C

34553623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41659566-G-T

34553687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41659627-C-T

http://identifiers.org/hco/9/GRCh38#34553693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41659640-A-C

34553853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41659802-G-A

34553924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41659873-G-A

34553976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41659926-G-C

http://identifiers.org/hco/9/GRCh38#34554092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41660048-C-A

34554092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41660048-C-T

34554492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41660384-C-G

34554899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41660776-G-A

34555001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41660873-T-C

34555045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41660917-G-A

34555113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41660991-C-T

34555196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41661073-G-A

34555212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41661089-G-A

http://identifiers.org/hco/9/GRCh38#34555804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41661676-A-C

34555817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41661689-G-A

34555878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41661730-G-C

http://identifiers.org/hco/9/GRCh38#34556125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41661838-C-A

34556135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41661848-G-A

34556135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41661848-G-C

34556135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41661848-G-T

34556321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: synonymous variant
orthologous variants: 41662039-G-A

34556321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: missense variant
orthologous variants: 41662039-G-C

34556484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41662197-G-A

34556484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41662197-G-T

http://identifiers.org/hco/9/GRCh38#34556543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41662243-C-A

http://identifiers.org/hco/9/GRCh38#34556544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41662244-C-A

34556576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41662275-T-C

34556614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41662312-A-G

34556614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41662312-A-T

34556647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41662343-C-T

34556792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41662471-C-T

34557172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41662892-C-T

34557385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41663101-A-G

34557415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41663122-T-G

34558188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41663869-G-A

34558356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41664042-T-C

34558744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41664441-G-C

34558878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41664551-A-G

34559081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41664745-T-C

34559363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41665013-G-C

34559363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41665013-G-T

34559466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41665095-C-T

34559700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41665250-G-A

34559777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41665360-G-A

34559777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41665360-G-C

34559777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41665360-G-T

34560012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41665558-C-T

34560386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41665917-G-T

34560681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41666504-C-T

34560715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41666548-C-T

34560753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41666586-C-T

34560826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41666655-C-T

http://identifiers.org/hco/9/GRCh38#34560902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41666731-C-A

34560902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41666731-C-T

http://identifiers.org/hco/9/GRCh38#34560933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41666762-C-A

34561077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41666907-C-G

34561179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41667008-G-A

http://identifiers.org/hco/9/GRCh38#34561277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41667089-A-C

34562105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41667869-A-G

34562167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41667915-C-G

34562167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41667915-C-T

34562532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41668373-G-C

34562815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41668767-C-T

34563358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41669273-G-A

34563359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41669274-G-T

34563441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41669358-G-A

34563441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41669358-G-T

34563488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41669537-T-C

34563565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41669770-A-G

34563794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41669957-A-G

34564042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41670246-C-G

34564042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41670246-C-T

http://identifiers.org/hco/9/GRCh38#34564489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41670740-C-A

34564489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41670740-C-T

http://identifiers.org/hco/9/GRCh38#34564528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41670778-C-A

34564528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41670778-C-T

34564529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41670779-T-A

34564821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: missense variant
orthologous variants: 41671065-C-T

34564898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41671143-G-A

34564898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41671143-G-T

34564919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41671154-T-A

34564919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41671154-T-C

34564940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41671163-G-A

34564940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41671163-G-T

http://identifiers.org/hco/9/GRCh38#34564996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41671210-C-A

34564996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41671210-C-T

34565041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41671255-A-G

34565255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41671441-A-G

34565291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41671473-C-T

http://identifiers.org/hco/9/GRCh38#34565363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41671548-C-A

34565577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41671788-G-A

34565599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41671806-T-A

34566504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41672715-G-T

http://identifiers.org/hco/9/GRCh38#34566685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41672904-C-A

34566738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41672959-G-A

34566886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41673125-T-C

34567322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41673477-C-T

34567378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41673533-C-T

34567938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41674094-G-T

34567983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41674129-A-G

34568301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674426-A-G

34568335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674463-T-C

34568345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674473-C-T

34568391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674515-A-T

34568460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674566-C-T

34568607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674696-C-T

34568611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674700-C-G

34568722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674830-G-T

34568842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674962-G-A

34568842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674962-G-T

34568869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674992-T-C

34568869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674992-T-G

http://identifiers.org/hco/9/GRCh38#34568873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41674996-C-A

34568873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674996-C-G

34568873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41674996-C-T

34569087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41675212-G-C

34569087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41675212-G-T

http://identifiers.org/hco/9/GRCh38#34569456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41675479-C-A

34569546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41675569-T-A

34569546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41675569-T-C

34569747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, splice_donor_variant, undefined
orthologous variants: 41675757-G-A

34569747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, splice_donor_variant, undefined
orthologous variants: 41675757-G-T

http://identifiers.org/hco/9/GRCh38#34569968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41675956-C-A

34569968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 41675956-C-T

34570876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41676708-G-A

34570910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41676747-G-T

http://identifiers.org/hco/9/GRCh38#34571244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41677033-C-A

34571244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41677033-C-T

http://identifiers.org/hco/9/GRCh38#34571262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41677051-C-A

34571262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41677051-C-G

34571359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41677141-C-T

34571423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41677213-A-G

http://identifiers.org/hco/9/GRCh38#34571491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41677274-C-A

34571491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41677274-C-T

34571540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41677359-G-A

34571631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41677451-C-G

34571631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41677451-C-T

http://identifiers.org/hco/9/GRCh38#34572559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41678219-C-A

34572815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41678459-C-T

34572921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41678516-C-T

34573050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41678644-C-T

http://identifiers.org/hco/9/GRCh38#34573197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41678789-C-A

34573407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41678963-G-A

34573809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 41679252-T-C

34573833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41679276-G-A

34573957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41679350-G-A

34574082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41679466-G-A

34574464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41679846-C-T

34574670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41680048-G-C

34574670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41680048-G-T

34575114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41680460-G-A

http://identifiers.org/hco/9/GRCh38#34575213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41680557-C-A

34575213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41680557-C-T

34576062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41681523-C-T

34576105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41681566-C-G

34576234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41681966-C-T

34576426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41682197-G-A

34576650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41682400-A-G

http://identifiers.org/hco/9/GRCh38#34576894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41682610-C-A

34577048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41682782-G-C

34577301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41683030-A-T

34577353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41683104-G-A

34577447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41683200-C-T

34577841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41683561-A-G

34578034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41683758-C-T

34578064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41683786-C-G

http://identifiers.org/hco/9/GRCh38#34578147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41683855-A-C

34578179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41683889-G-A

34578179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41683889-G-C

34578237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41683918-G-A

34578237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41683918-G-T

http://identifiers.org/hco/9/GRCh38#34578597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41684212-C-A

34578597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41684212-C-G

34578804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41684421-G-A

34578804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41684421-G-T

34578843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41684458-C-T

34579032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41684668-G-C

34579117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41684749-C-T

34579199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41684832-T-G

34579284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41684918-G-A

34579284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41684918-G-C

http://identifiers.org/hco/9/GRCh38#34580081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41685744-C-A

http://identifiers.org/hco/9/GRCh38#34580086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41685748-C-A

34580099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, splice_acceptor_variant, undefined
orthologous variants: 41685761-G-T

http://identifiers.org/hco/9/GRCh38#34580135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41685797-C-A

34580135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41685797-C-T

34580169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41685821-A-G

34580237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41685886-T-C

34580259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41685906-G-A

34580298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41685950-T-C

34580328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41685980-A-G

34580372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41686020-C-T

34580549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41686245-G-A

34580573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41686269-G-A

34580573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41686269-G-C

http://identifiers.org/hco/9/GRCh38#34580577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41686273-C-A

34580577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41686273-C-T

http://identifiers.org/hco/9/GRCh38#34581056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41686757-C-A

34581066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41686767-A-G

34581131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41686833-T-C

34581134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41686836-T-C

http://identifiers.org/hco/9/GRCh38#34581194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41686875-C-A

34581194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41686875-C-T

34581195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41686876-A-G

34581197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41686878-G-T

http://identifiers.org/hco/9/GRCh38#34581222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41686903-C-A

34581222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41686903-C-T

34581254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41686931-C-T

34581277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41686947-C-T

34581498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41687329-A-G

34581567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41687422-G-A

34581684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41687533-T-C

http://identifiers.org/hco/9/GRCh38#34581860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41687750-C-A

http://identifiers.org/hco/9/GRCh38#34582114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41688197-A-C

34582221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41688327-G-T

http://identifiers.org/hco/9/GRCh38#34582368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41688517-C-A

34582379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41688528-T-C

34582610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41688739-T-C

34582670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41688794-G-A

34582670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41688794-G-T

http://identifiers.org/hco/9/GRCh38#34582766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41688884-C-A

34582766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41688884-C-T

34582873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41688989-G-T

34582966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41689077-G-A

34582966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41689077-G-T

34582968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41689079-G-A

34582968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41689079-G-C

34582968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41689079-G-T

34583004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41689109-C-T

34583209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41689335-C-T

34583251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41689376-C-T

34583470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41689595-C-T

34583829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41689911-C-T

34583839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41689921-C-T

34584860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41690803-G-C

34585217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41691114-G-A

34585554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41691407-G-C

34585778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41691609-A-G

34585908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41691743-C-T

34585956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41691790-G-A

34586725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41692476-G-T

34586807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41692549-T-C

34586839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41692592-C-T

34586986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41692698-G-C

http://identifiers.org/hco/9/GRCh38#34587341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41693045-A-C

34587341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41693045-A-G

http://identifiers.org/hco/9/GRCh38#34587347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41693051-C-A

34587573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41693263-T-A

34587573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41693263-T-C

34587731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41693465-G-A

34587746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41693480-G-A

34587784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41693531-G-A

34587885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41693613-T-G

34587925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41693648-G-A

34587930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41693653-G-A

34588102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41693848-G-A

34589046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41694738-G-A

34589169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41694872-G-C

34589189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41694892-G-A

34589979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41695746-G-A

34589979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41695746-G-T

34589980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron variant
orthologous variants: 41695747-G-T

34590015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41695782-G-A

34590015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41695782-G-T

http://identifiers.org/hco/9/GRCh38#34590019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41695786-C-A

34590019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: intron_variant, undefined
orthologous variants: 41695786-C-T

34590143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41695908-G-A

34590143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41695908-G-T

http://identifiers.org/hco/9/GRCh38#34590232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41695985-C-A

34590232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 41695985-C-G

34590232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 41695985-C-T

34590296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2170
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41696040-C-T