246566568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 179374086-A-G

246566604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179374122-G-A

246566604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179374122-G-T

246566620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179374138-A-G

246566684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179374200-A-G

246566735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179374248-T-C

http://identifiers.org/hco/1/GRCh38#246566809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#179374296-C-A

246566809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179374296-C-T

246567114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179374567-C-G

246567671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179375097-T-C

246567671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179375097-T-G

246569154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179376649-A-G

246569197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179376695-A-G

246569560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179377063-T-G

246569755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179377105-C-T

http://identifiers.org/hco/1/GRCh38#246569769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179377119-C-A

246570118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179377488-C-T

246570265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179377611-C-T

246570888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179378701-C-T

246571593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179379108-T-C

246571626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179379136-T-G

http://identifiers.org/hco/1/GRCh38#246571988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179379461-C-A

246571988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179379461-C-G

246572043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179379514-A-G

246577045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179387204-G-T

246577302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179387630-C-G

246577302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179387630-C-T

246577320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179387648-A-G

246577382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179387718-T-C

246577436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179387847-A-G

246577939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179388583-C-G

246578083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179388726-A-G

246578145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179388788-A-G

246578362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179388967-G-T

246578996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179389273-G-A

246578998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179389275-A-G

246579108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179389369-T-C

246579121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179389380-T-G

246579331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179389551-A-G

246579406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179389626-T-C

246580037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179391721-T-G

246582988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179395293-G-C

246583052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179395354-C-T

246583410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179396197-G-C

246583539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179396290-A-T

246583654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179396402-T-A

246583828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179396560-G-A

246584464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179397537-G-A

246584509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179397583-T-A

246584516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179397588-G-A

246588501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179398215-G-T

246591371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179406782-G-T

246591434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179406825-A-G

246591434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179406825-A-T

246591445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179406836-A-G

246591455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179406846-A-T

246591635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179407027-G-A

246591700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179407092-C-T

246591789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179407181-C-T

246591916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179407308-A-G

246591917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179407309-G-C

246591931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179407323-G-T

246591933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179407325-T-A

246591933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179407325-T-C

246592054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179407388-G-T

246592150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179407480-T-C

246592634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179407538-A-T

246592714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179407618-G-A

246592719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179407623-A-G

246592807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179407688-A-G

246592828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179407705-C-T

246592948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179407858-C-T

246592950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179407860-A-G

246593069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179407986-T-C

246596717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179408837-C-T

246596843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179408951-C-T

246597006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179409117-A-G

246597359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179409449-C-T

246597397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179409487-C-T

246597500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179409591-C-T

246597576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179409667-G-A

246597592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179409674-A-G

246597592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179409674-A-T

246598421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179410162-C-T

246598442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179410183-C-G

246598492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179410233-T-C

246599455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179410730-T-C

246599841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411065-G-A

246599841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411065-G-T

246599864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411087-A-G

246599938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411162-G-T

246599984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411204-A-G

246600023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411240-G-T

246600125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411331-G-A

246600191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411375-G-A

246600222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411404-A-G

246600314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411488-G-A

246600385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411552-T-C

246600385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411552-T-G

246600396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179411560-T-G

246604447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179412229-G-C

246604459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179412241-G-A

246605094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179412661-G-A

246605101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179412668-T-C

246605218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179412775-A-T

http://identifiers.org/hco/1/GRCh38#246608512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179413004-C-A

http://identifiers.org/hco/1/GRCh38#246608531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179413023-C-A

246609172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179414576-A-G

246614990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179416023-G-A

246615980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179416317-T-C

246616052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179416383-T-G

246616191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179416525-G-A

246617155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179416910-A-T

246621048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179419361-G-C

http://identifiers.org/hco/1/GRCh38#246621180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179419492-C-A

246621219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179419530-A-G

http://identifiers.org/hco/1/GRCh38#246621305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179419597-C-A

246621305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179419597-C-T

246621344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179419636-G-T

http://identifiers.org/hco/1/GRCh38#246621352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179419644-C-A

246621383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179420205-T-C

246621441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179420250-G-A

246621535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179420338-G-C

246622051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179420477-G-C

246622094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179420512-C-T

246622340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179420754-G-C

246622464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179420872-C-T

http://identifiers.org/hco/1/GRCh38#246622772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179422016-A-C

246624491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179423844-A-G

246624547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179423897-C-T

246624580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179423912-C-T

246624655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179423985-G-A

246624755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179424285-T-A

246631653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179429051-A-G

246631676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179429077-A-G

246631770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179429162-A-T

http://identifiers.org/hco/1/GRCh38#246631845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179429232-C-A

246631952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179429323-A-G

http://identifiers.org/hco/1/GRCh38#246631964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179429335-C-A

246631964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179429335-C-G

246631971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179429342-A-G

246631971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179429342-A-T

http://identifiers.org/hco/1/GRCh38#246632108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179429470-C-A

http://identifiers.org/hco/1/GRCh38#246632154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179429516-C-A

246632154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179429516-C-T

http://identifiers.org/hco/1/GRCh38#246632575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179431185-A-C

246632575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179431185-A-G

246632575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179431185-A-T

http://identifiers.org/hco/1/GRCh38#246632674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179431283-C-A

246632780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179431392-G-A

246632780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179431392-G-T

246632888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179431502-A-G

246632979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179431583-A-G

http://identifiers.org/hco/1/GRCh38#246633066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#179431668-C-A

246633091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179431688-T-C

http://identifiers.org/hco/1/GRCh38#246633783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179431780-A-C

246633783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179431780-A-T

246633918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 179432078-A-G

246633956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 179432116-C-T

246634034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179432194-G-A

http://identifiers.org/hco/1/GRCh38#246634044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179432204-C-A

246634044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179432204-C-T

246634393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179432467-G-A

246634393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179432467-G-T

246634435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179432480-T-A

246634435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179432480-T-G

246634442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179432487-A-T

246634449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179432494-G-C

246634449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179432494-G-T

http://identifiers.org/hco/1/GRCh38#246634450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179432495-A-C

246634510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179432555-G-A

246634535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179432580-T-C

246634624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179432669-T-A

246634633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179432675-G-C

246634645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179432687-T-C

246634674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179432732-T-A

246634674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179432732-T-C

246634709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179432767-T-C

246641099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179433275-C-T

246641277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179433446-G-T

246641534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179433612-A-G

246641597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179433674-A-G

246641621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179433698-A-G

246641629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179433706-T-C

http://identifiers.org/hco/1/GRCh38#246641644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179433721-C-A

http://identifiers.org/hco/1/GRCh38#246641670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179433746-C-A

246641670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179433746-C-T

246641835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179433897-G-A

246641835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179433897-G-T

http://identifiers.org/hco/1/GRCh38#246641837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179433899-A-C

246641837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179433899-A-G

246641943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 179434004-A-G

246641982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179434043-G-A

246641987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 179434048-T-G

246642041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179434102-T-C

246642041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179434102-T-G

246642063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179434120-G-A

246642063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179434120-G-T

http://identifiers.org/hco/1/GRCh38#246642099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179434154-C-A

246642099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179434154-C-G

246642099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179434154-C-T

246642530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179434567-T-C

246643414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179435709-C-T

246643654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179435940-C-T

246646849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179437077-A-T

http://identifiers.org/hco/1/GRCh38#246647059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179437271-A-C

246647071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179437283-C-G

246647071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179437283-C-T

http://identifiers.org/hco/1/GRCh38#246647091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179437302-C-A

246647095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179437306-G-T

246647107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179437318-A-G

246647127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179437339-C-T

http://identifiers.org/hco/1/GRCh38#246647155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179437367-C-A

246647155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179437367-C-T

246647156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437368-G-A

246647156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437368-G-T

246647219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437428-C-G

246647230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179437439-C-T

246647260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179437469-A-G

246647260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179437469-A-T

246647317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179437526-G-A

246647317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179437526-G-T

246647345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437554-G-A

246647374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179437583-G-A

246647374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437583-G-C

246647399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179437608-T-C

246647513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437704-G-C

246647522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437713-C-G

246647522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437713-C-T

246647523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437714-G-A

246647523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437714-G-C

246647610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437801-C-T

246647611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179437802-G-A

246647628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437819-T-C

246647634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437825-A-G

246647652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437843-T-G

http://identifiers.org/hco/1/GRCh38#246647700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179437891-A-C

246647700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437891-A-G

246647715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437909-G-A

246647715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437909-G-C

246647715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437909-G-T

246647786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179437980-G-A

http://identifiers.org/hco/1/GRCh38#246647857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179438051-A-C

246647857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179438051-A-G

246647869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179438063-A-G

246647869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 179438063-A-T

246647896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179438090-T-C

246648198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179438351-A-G

246648198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179438351-A-T

http://identifiers.org/hco/1/GRCh38#246648243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179438397-C-A

246648243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 179438397-C-G

246648243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 179438397-C-T

246648270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179438424-T-C

246648287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179438450-T-C

246648322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179438479-G-A

246648322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179438479-G-T

http://identifiers.org/hco/1/GRCh38#246648324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179438481-C-A

246648324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179438481-C-T

246648351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179438508-G-T

http://identifiers.org/hco/1/GRCh38#246648391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179438543-C-A

246648391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179438543-C-T

246648412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179438565-A-G

246648447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179438601-A-G

246650332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440130-A-G

246650375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440168-T-G

246650547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440311-T-A

246650547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440311-T-G

246650564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440328-T-C

246650648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440365-A-T

246650698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440413-T-C

246650698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440413-T-G

246650702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440417-G-A

246650702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440417-G-T

246650714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440426-G-T

246650716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440428-C-T

246650823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440519-A-G

246650895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440586-C-T

246650930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440613-G-A

246650930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440613-G-C

246651097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440779-C-G

246651335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440895-C-T

246651475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179440993-C-T

246651487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179441005-G-A

246651612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179441099-T-C

246651759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179441253-G-A

246653436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179441967-A-G

246653571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179442090-T-C

246653626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179442199-C-T

246653678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179442250-G-T

http://identifiers.org/hco/1/GRCh38#246653793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179442358-A-C

246654186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179443011-G-T

246654217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179443080-C-G

http://identifiers.org/hco/1/GRCh38#246654318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179443221-C-A

246654480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179443332-A-G

http://identifiers.org/hco/1/GRCh38#246655126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179444037-C-A

246655208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179444114-A-G

246655362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179444434-G-A

246655432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179444502-A-T

246655443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179444521-A-G

246655902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179444885-A-G

246656203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179445005-T-C

246656424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179445203-T-A

246658670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449008-A-G

246658815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449101-T-C

246658890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449185-G-A

246658890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449185-G-C

246658892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449187-T-C

246659085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449351-G-A

246659104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449364-G-A

246659104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449364-G-C

246659154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449418-C-T

http://identifiers.org/hco/1/GRCh38#246659187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179449489-A-C

246659382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449763-C-G

246659526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449880-C-T

246659670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449975-G-A

246659674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179449976-A-G

246660154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179450289-T-C

246660161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179450296-T-C

246660210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: synonymous variant
orthologous variants: 179450343-T-A

246660210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: synonymous variant
orthologous variants: 179450343-T-C

http://identifiers.org/hco/1/GRCh38#246660350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179450484-C-A

246660829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179450614-A-G

246660927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179450746-T-G

246660931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: intron variant
orthologous variants: 179450750-T-C

246665707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: synonymous variant
orthologous variants: 179452571-T-C

246665802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense variant
orthologous variants: 179452666-T-C

246665861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: missense variant
orthologous variants: 179452725-C-T

246665949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179452815-G-A

http://identifiers.org/hco/1/GRCh38#246665997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179452863-C-A

246666009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179452875-T-C

246666118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179452956-G-A

246666118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179452956-G-T

246666328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179453107-A-G

246666328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179453107-A-T

246666412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179453193-T-G

http://identifiers.org/hco/1/GRCh38#246666495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179453268-C-A

246666546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179453323-A-T

246666557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179453334-G-C

246666557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179453334-G-T

246666661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179453417-A-G

246666828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179453588-C-T

246666896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179453649-T-C

246667311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179454048-G-C

246667421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179454154-G-A

246667421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179454154-G-T

http://identifiers.org/hco/1/GRCh38#246667664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179454392-A-C

http://identifiers.org/hco/1/GRCh38#246667852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#179454566-C-A

246667873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179454593-G-C

246668060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179454766-G-A

246668138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179454844-T-C

246668455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26486
most severe consequence: 3 prime UTR variant
orthologous variants: 179455152-G-A