43358933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 94237030-G-A

http://identifiers.org/hco/11/GRCh38#43358991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#94236972-C-A

43358991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 94236972-C-T

43359152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94236816-T-A

43359152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94236816-T-C

http://identifiers.org/hco/11/GRCh38#43359186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94236782-C-A

43359186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94236782-C-G

43359186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94236782-C-T

http://identifiers.org/hco/11/GRCh38#43359272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94236705-C-A

43359272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94236705-C-G

43359272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94236705-C-T

http://identifiers.org/hco/11/GRCh38#43359300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#94236677-C-A

43359300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94236677-C-T

43359302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94236675-G-T

43359305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94236672-C-T

http://identifiers.org/hco/11/GRCh38#43359316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94236661-C-A

43359316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94236661-C-G

43359316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94236661-C-T

43359559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94236431-C-G

43359815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94236174-C-G

43359988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94235926-T-C

43360403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94235552-C-T

43360406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94235549-T-A

43360406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94235549-T-G

43360467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94235472-C-G

43360508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94235427-T-C

http://identifiers.org/hco/11/GRCh38#43360522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94235413-C-A

43360522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94235413-C-G

43360601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94235334-A-G

43360609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94235326-G-T

43360682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94235249-A-G

43360745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94235181-C-T

43362796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94233863-G-A

43362887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94233794-A-G

43362888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94233793-G-A

43362989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94233708-T-C

43363039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94233653-A-T

43363049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94233643-C-T

43363449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94232158-T-C

http://identifiers.org/hco/11/GRCh38#43363684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94231934-A-C

43363684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231934-A-G

43364011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231609-C-T

43364032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231588-C-T

http://identifiers.org/hco/11/GRCh38#43364039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94231581-C-A

43364039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231581-C-T

43364378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231404-G-A

43364444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231341-C-G

43367287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94229447-A-G

http://identifiers.org/hco/11/GRCh38#43367374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94229366-A-C

43367424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94229327-A-G

43367440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94229311-A-T

43367822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228977-C-T

43367887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228901-C-G

43368491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228504-T-C

43368533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228463-A-G

43368690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228326-C-T

43368740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228276-C-T

43368875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228152-G-A

43368879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94228148-T-G

43369152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94225839-A-G

43370098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94225039-C-T

43370114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94225023-G-A

http://identifiers.org/hco/11/GRCh38#43370213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94224934-C-A

43370213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94224934-C-G

43370213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94224934-C-T

43370269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94224877-C-G

43370674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94224292-A-G

http://identifiers.org/hco/11/GRCh38#43375004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94219746-A-C

43375004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94219746-A-G

http://identifiers.org/hco/11/GRCh38#43375064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94219687-C-A

http://identifiers.org/hco/11/GRCh38#43375141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94219637-C-A

43375141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94219637-C-T

43375259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94219545-C-T

http://identifiers.org/hco/11/GRCh38#43375270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94219534-A-C

43375659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94219188-G-T

43375784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94219074-G-A

43376201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94218593-T-A

43376201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94218593-T-C

43376483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94218330-A-G

43376671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94218057-T-C

43376679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94218045-A-G

43376747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217992-T-G

43377422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217915-G-T

43377505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217830-A-G

43377505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217830-A-T

43377587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217758-C-T

43377624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217721-C-T

43377650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217694-G-C

43377654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217683-C-T

43377877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217481-G-A

43378404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217319-G-A

43378531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217198-T-G

43378622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217105-T-A

43378622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94217105-T-C

43378821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94216908-A-G

43378864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94216864-A-G

43378873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94216855-A-G

43378877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94216851-G-A

43378877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94216851-G-T

http://identifiers.org/hco/11/GRCh38#43378878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94216850-C-A

43378878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94216850-C-T

43378906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94216819-T-C

43378906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94216819-T-G

43378920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94216805-A-G

http://identifiers.org/hco/11/GRCh38#43378956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94216770-C-A

43378956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94216770-C-G

43378973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94216757-A-G

43379073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94216678-A-G

http://identifiers.org/hco/11/GRCh38#43379078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94216673-C-A

43379078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94216673-C-T

43379148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94216613-A-G

43379205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94216557-G-A

43379205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94216557-G-C

43379205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94216557-G-T

43379786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94215671-T-G

43381124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94213281-T-C

43381236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94213219-C-T

43381368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94213090-T-C

43389742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94209111-T-A

43389895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94208977-T-C

http://identifiers.org/hco/11/GRCh38#43389959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94208918-C-A

http://identifiers.org/hco/11/GRCh38#43389963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94208916-A-C

43389963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94208916-A-G

43390837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94208738-T-C

43391610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94208270-G-T

43391621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94208259-T-A

43391621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94208259-T-C

43391621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94208259-T-G

43391644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94208231-A-T

43391779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94208114-A-G

43392000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94207908-C-T

http://identifiers.org/hco/11/GRCh38#43392032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94207879-A-C

43392114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94207797-G-A

http://identifiers.org/hco/11/GRCh38#43392270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94207656-C-A

43392284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94207642-T-G

43392391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94207416-T-G

43396551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94206629-T-C

43396640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94206559-G-A

43396640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94206559-G-T

http://identifiers.org/hco/11/GRCh38#43396641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94206558-C-A

43396641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94206558-C-G

43396687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94206504-A-G

43396835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94206356-T-C

43396856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94206333-T-C

43396863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94206326-G-T

http://identifiers.org/hco/11/GRCh38#43396905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94206286-C-A

43396905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94206286-C-T

http://identifiers.org/hco/11/GRCh38#43396926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94206261-C-A

43396926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94206261-C-G

43396926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94206261-C-T

43396976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94206214-A-G

43397041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94206155-T-C

43397059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94206132-T-C

43397059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94206132-T-G

43397082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94206091-T-G

43397111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94205760-A-G

http://identifiers.org/hco/11/GRCh38#43397191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94205680-C-A

http://identifiers.org/hco/11/GRCh38#43397303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94205632-C-A

43397303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94205632-C-G

43397303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94205632-C-T

43397331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94205605-G-T

http://identifiers.org/hco/11/GRCh38#43397372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94205544-A-C

43397602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94205311-A-T

43397637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94205273-T-C

43397919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94205022-T-G

43398016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94204958-G-A

43398143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94204831-A-G

43398143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94204831-A-T

43398150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94204824-C-T

43398166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94204808-T-G

43398198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94204776-G-A

43398198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94204776-G-T

http://identifiers.org/hco/11/GRCh38#43398222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94204754-C-A

43398222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94204754-C-T

43398230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94204746-T-A

43398230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94204746-T-G

http://identifiers.org/hco/11/GRCh38#43398241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94204739-C-A

43398342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94204661-G-A

43398958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94203595-T-C

43399110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94203472-G-C

43399158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94203440-G-A

43399750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94202359-G-A

43399817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94202310-G-A

43400150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94202000-T-G

43400154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94201996-T-C

43400154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94201996-T-G

43400157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94201391-G-A

43400157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94201391-G-C

43400378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94201216-T-C

43400549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94200876-C-T

43400750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94200616-A-T

43400886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94200475-C-T

43401422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94199790-G-A

43401422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94199790-G-T

43401468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94199746-G-A

43402427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94199033-T-A

43402541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94198908-A-G

43403043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94198184-C-T

43403048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94198179-A-G

43403359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94197915-T-G

43403480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94197801-G-A

43403862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94197140-A-G

43403862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94197140-A-T

http://identifiers.org/hco/11/GRCh38#43404208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94196801-C-A

43404208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94196801-C-T

http://identifiers.org/hco/11/GRCh38#43404708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94196371-C-A

43405121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94196031-G-T

43405127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94196025-C-T

43405337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94195843-G-A

43406355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94194255-T-C

43406528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94194040-A-G

43406547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94194020-C-T

http://identifiers.org/hco/11/GRCh38#43406639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94193938-C-A

43406676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94193899-A-G

43406678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94193897-G-T

43406703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94193874-G-T

43406749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94193830-C-T

43406882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94193699-A-T

43406923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94193675-G-T

43407048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94193512-G-A

43407048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94193512-G-T

43407127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94193132-T-C

http://identifiers.org/hco/11/GRCh38#43407536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94192724-A-C

43407536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94192724-A-G

http://identifiers.org/hco/11/GRCh38#43408364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94191326-A-C

43408391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94191303-G-A

43408403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94191291-A-G

43408488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94191215-G-A

43408504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94191189-G-A

43408570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94191134-T-A

43414354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94189504-A-G

http://identifiers.org/hco/11/GRCh38#43414454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94189420-A-C

43414454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94189420-A-G

43414485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94189388-T-A

43414527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94189346-C-T

http://identifiers.org/hco/11/GRCh38#43414569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94189306-C-A

43414571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94189304-G-A

43414571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94189304-G-T

43414580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94189295-T-C

http://identifiers.org/hco/11/GRCh38#43414816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94189063-C-A

43414819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94189060-G-C

43414819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94189060-G-T

43414880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94189001-T-C

http://identifiers.org/hco/11/GRCh38#43414898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94188988-C-A

http://identifiers.org/hco/11/GRCh38#43414956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94188938-A-C

43414956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94188938-A-T

43415181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94188744-T-G

43415488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94188531-G-A

43415488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94188531-G-C

43415488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94188531-G-T

43415594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94188438-C-G

43416113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94187927-G-A

43416642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94187420-A-G

43419348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94185871-G-A

43420082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94185466-C-G

43420335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94185095-G-A

http://identifiers.org/hco/11/GRCh38#43420396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94185034-A-C

43420425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94185005-G-A

43420432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94184998-G-A

43420820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94183697-C-T

43420845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94183672-A-G

43426630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94182275-A-G

43426876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94182042-C-G

43428007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94181067-C-G

43428046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94181032-C-T

http://identifiers.org/hco/11/GRCh38#43428190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94180909-C-A

43428190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94180909-C-G

43428319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94180798-C-G

43428430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94180677-T-C

http://identifiers.org/hco/11/GRCh38#43428457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94180665-C-A

43428804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94180291-G-A

43428804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94180291-G-T

http://identifiers.org/hco/11/GRCh38#43428912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94180169-C-A

43428948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94180133-T-A

43429109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94179951-C-G

43431518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94177529-C-T

43431574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94177471-A-G

43432110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94177100-T-C

43432110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94177100-T-G

43432405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94176788-A-G

43432463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94176732-G-A

43432557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94176639-T-C

43432718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94176386-T-G

43432958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94176119-A-T

43433427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94175778-C-T

43433566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94175652-T-G

43434085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94175216-C-T

43434384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174772-A-G

43434568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174507-A-G

43434579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174493-T-C

43434614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174458-A-G

43434662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174410-C-G

http://identifiers.org/hco/11/GRCh38#43434675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94174397-A-C

43434747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174316-C-G

43434747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174316-C-T

43434872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174212-A-G

http://identifiers.org/hco/11/GRCh38#43435343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94174047-C-A

43435343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94174047-C-T

43435675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94173578-C-T

http://identifiers.org/hco/11/GRCh38#43436047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94173256-C-A

43436262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94173042-A-G

43436299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94173005-A-G

43436408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172896-A-G

43436408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172896-A-T

http://identifiers.org/hco/11/GRCh38#43436469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94172819-C-A

43436469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172819-C-G

43436469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172819-C-T

43436471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172817-T-C

43436472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172816-A-T

43436551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172771-T-C

http://identifiers.org/hco/11/GRCh38#43436556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94172766-A-C

43436877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172700-A-G

43437035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172564-C-T

43437425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172168-T-G

43437512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172045-T-C

43438932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167602-G-A

43438950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167578-G-A

43439091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167453-T-C

43439092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167452-A-G

43439378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167178-C-T

43440081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94166839-A-G

43440228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94166699-G-A

43440391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94166541-T-C

43440630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94166372-T-G

http://identifiers.org/hco/11/GRCh38#43440669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94166337-C-A

http://identifiers.org/hco/11/GRCh38#43440756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94166260-A-C

43440832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94166207-T-C

43441348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94166028-C-T

http://identifiers.org/hco/11/GRCh38#43441460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94165928-C-A

http://identifiers.org/hco/11/GRCh38#43441601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94165783-C-A

43441601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94165783-C-G

43441755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94165641-C-G

43441868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94165513-C-T

http://identifiers.org/hco/11/GRCh38#43442551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94164100-A-C

43443183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94163532-G-A

43443183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94163532-G-T

http://identifiers.org/hco/11/GRCh38#43443247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94163470-A-C

43443247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94163470-A-G

43443367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94163353-A-G

43443373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94163347-A-G

43443459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94163261-G-A

43443495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94163225-C-T

43444167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94160903-C-G

43444167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94160903-C-T

43444179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94160891-G-A

43444256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94160817-T-C

43444600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94160150-T-C

43444668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94160088-A-G

43444875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159934-T-C

43444890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159919-G-A

http://identifiers.org/hco/11/GRCh38#43444924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94159886-A-C

43444965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159848-A-G

43444980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159833-T-C

43445021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159792-A-G

43445061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159767-G-A

43445074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159754-A-G

43445207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159639-C-T

43445404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159454-A-G

43445404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159454-A-T

43445455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159404-T-C

43445476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159386-T-C

http://identifiers.org/hco/11/GRCh38#43445547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94159321-A-C

43445703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159067-T-C

http://identifiers.org/hco/11/GRCh38#43445796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94158976-C-A

43445851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94158920-T-G

http://identifiers.org/hco/11/GRCh38#43445867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94158904-C-A

43445897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94158874-A-G

43446570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94158234-T-C

43446588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94158224-A-G

43446589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94158223-G-C

43446589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94158223-G-T

43446697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94158116-A-G

43446697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94158116-A-T

43446700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94158113-A-G

43446712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94158101-A-G

43446814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94158011-A-G

http://identifiers.org/hco/11/GRCh38#43446823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94158002-C-A

43446823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94158002-C-T

43447054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94157914-T-C

43447564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94157609-A-G

43447724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94157447-A-T

http://identifiers.org/hco/11/GRCh38#43447827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94157342-C-A

43447827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94157342-C-T

43447863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94157299-T-C

43447863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94157299-T-G

http://identifiers.org/hco/11/GRCh38#43447869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94157293-A-C

43447869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94157293-A-G

43447869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94157293-A-T

43447894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94157266-T-C

43447937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94157225-G-A

43447953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94157209-G-T

43448142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94157021-C-G

43448142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94157021-C-T

http://identifiers.org/hco/11/GRCh38#43448195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94156959-C-A

43448195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94156959-C-G

43448208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94156942-G-A

43448219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94156931-A-T

43448274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94156894-T-C

43448279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94156889-C-G

43448446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94156747-T-C

http://identifiers.org/hco/11/GRCh38#43448592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94156641-C-A

43448592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94156641-C-G

43448663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94156580-A-G

43449882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94155018-G-T

43450209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94154737-C-G

http://identifiers.org/hco/11/GRCh38#43450218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94154728-A-C

43450282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94154660-A-G

43450326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94154617-G-A

43450326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94154617-G-T

http://identifiers.org/hco/11/GRCh38#43450329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94154614-C-A

43450839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153875-G-A

43450998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153696-G-A

43451032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153663-T-C

43451115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153582-A-G

http://identifiers.org/hco/11/GRCh38#43451135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94153562-C-A

43451135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153562-C-G

43451135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153562-C-T

43451175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94153522-C-T

http://identifiers.org/hco/11/GRCh38#43451301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94153398-C-A

43451301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153398-C-T

43451360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153347-A-G

43451360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153347-A-T

43451385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153328-A-G

43451403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153310-T-G

43451436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153278-A-G

43451463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94153247-T-C

43451824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94152914-A-G

43452023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94152717-G-A

43461550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94149453-C-G

43462033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94148995-A-G

43462371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94148698-A-G

43462681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94148423-A-G

43462779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94148331-T-C

43462779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94148331-T-G

43463414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94148021-A-G

43463591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147881-T-C

43463853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147632-A-G

43464459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147371-C-T

43464465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147365-G-A

http://identifiers.org/hco/11/GRCh38#43464572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94147266-A-C

43464580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147258-T-C

43464750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147120-A-G

43464802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147091-C-G

43465071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146857-T-C

43465102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146830-G-T

43465254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146534-T-A

43465382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146341-A-G

43465479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146242-A-G

43465551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146176-G-A

43465639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146083-A-G

43466101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94145728-T-C

43466243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94145612-T-A

43466295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94145570-A-G

43466301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94145562-T-C

43466311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94145552-G-A

43467150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94145456-G-A

http://identifiers.org/hco/11/GRCh38#43467285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94145322-A-C

43467386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94145248-G-A

43467403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94145232-A-G

http://identifiers.org/hco/11/GRCh38#43467890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94144816-C-A

43467890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94144816-C-T

43467912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94144806-A-T

43467917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94144801-G-A

43468010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94144709-G-T

43468112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94144632-A-G

43470424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94142781-C-T

43470743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94142545-C-T

43470778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94142510-G-A

43471246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94142028-G-C

43471342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141927-G-C

43490191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94135453-G-A

43490191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94135453-G-T

43490193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94135451-G-A

43490193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94135451-G-C

http://identifiers.org/hco/11/GRCh38#43490311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94135334-A-C

43490311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94135334-A-G

43490706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94135119-T-C

43491000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134950-A-T

43491013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134937-G-C

43491013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134937-G-T

43491181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134783-G-T

43491195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134769-A-G

43491212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134744-G-T

43491215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134741-T-A

http://identifiers.org/hco/11/GRCh38#43491258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94134703-A-C

43491258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134703-A-G

http://identifiers.org/hco/11/GRCh38#43491360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94134617-C-A

43491379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134607-G-A

43491421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134598-G-A

43491421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134598-G-T

43491778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134159-G-A

43491778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134159-G-C

43491778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134159-G-T

43491829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134131-A-G

43491829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134131-A-T

43491943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94134078-T-A

http://identifiers.org/hco/11/GRCh38#43492071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94133980-A-C

43492309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133756-G-A

43492309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133756-G-T

43492311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133754-A-G

43492321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133744-G-A

43492585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133377-A-G

43492663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133287-C-T

43492848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133008-C-T

43492921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94132950-A-G

43493110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94132761-G-A

43493582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94132360-A-G

43493597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94132345-A-G

http://identifiers.org/hco/11/GRCh38#43493708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94132272-A-C

43493718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94132263-A-G

http://identifiers.org/hco/11/GRCh38#43493738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94132243-C-A

43493806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94132177-T-C

43493869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94132114-C-T

43493896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94132087-T-C

http://identifiers.org/hco/11/GRCh38#43493908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94132075-A-C

43493908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94132075-A-G

43493930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94132051-T-C

43493977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94132020-G-A

43493977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94132020-G-T

43494001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94131997-G-A

43494001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94131997-G-T

43494094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94131906-T-A

43494094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94131906-T-C

43494094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94131906-T-G

http://identifiers.org/hco/11/GRCh38#43494228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94131797-C-A

43494231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94131796-A-G

http://identifiers.org/hco/11/GRCh38#43494304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94131729-C-A

43494304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94131729-C-T

http://identifiers.org/hco/11/GRCh38#43494366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94131669-C-A

43494400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94131636-T-C

43494815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94131228-T-A

43494839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94131205-T-C

http://identifiers.org/hco/11/GRCh38#43494863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25596
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94131181-A-C