173168820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58106026-T-C

173168822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58106024-G-A

173169047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 58105763-G-A

173169047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 58105763-G-C

173169047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 58105763-G-T

173169091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105721-G-A

173169219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105555-G-A

173169219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105555-G-T

173169222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105552-G-A

173169222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105552-G-T

173169224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105550-G-A

173169224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105550-G-C

173169224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105550-G-T

http://identifiers.org/hco/4/GRCh38#173169226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58105548-C-A

173169226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105548-C-G

173169226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105548-C-T

http://identifiers.org/hco/4/GRCh38#173169229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58105545-C-A

173169229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105545-C-G

173169229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105545-C-T

173169289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105481-C-T

173169564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58105241-A-T

173169775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58105063-G-A

http://identifiers.org/hco/4/GRCh38#173169800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#58105037-C-A

173169826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58105011-C-T

173169827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58105010-T-A

173169832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58105005-C-T

173169860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58104977-G-A

173170140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58104741-G-A

173170174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58104700-G-A

173170236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58104626-C-T

173170478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58104420-G-A

173170478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58104420-G-C

173170498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58104397-A-T

173170714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58104259-A-G

173170714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58104259-A-T

173170716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58104257-A-G

http://identifiers.org/hco/4/GRCh38#173170734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58104225-C-A

173170734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58104225-C-G

173170862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58104099-C-T

173170872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58104078-G-A

173171511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58103389-T-A

173171658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58103296-C-T

173171878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58102893-A-G

173171904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58102867-G-A

173172857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58102294-A-G

173172872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58102278-T-A

173173379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58101851-G-A

173173379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58101851-G-C

173173702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58101741-T-G

173173843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58101620-T-C

173173862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58101602-G-C

173174187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58101331-T-C

173174665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58100790-C-G

173174824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58100247-G-A

173174923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58100137-A-G

173174927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58100134-G-A

173174993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58100066-T-C

173176765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58097294-T-A

http://identifiers.org/hco/4/GRCh38#173176808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58097285-C-A

173177763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58096901-G-A

173177772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58096892-G-C

173177818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58096839-C-T

173177902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58096765-T-G

173178120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58096609-A-G

173178165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58096556-C-T

173178342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58096401-A-G

173178348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58096395-A-G

173178392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58096313-A-G

173178454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58096254-A-G

173178588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58096121-G-A

173178662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58096049-T-C

173178850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58095855-A-T

173178881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58095822-C-T

http://identifiers.org/hco/4/GRCh38#173178887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58095816-A-C

173178903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58095800-T-C

173178926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58095782-A-G

173178926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58095782-A-T

http://identifiers.org/hco/4/GRCh38#173180944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58093410-A-C

173180944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58093410-A-G

173181102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58093250-A-G

173181119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58093233-T-C

173181142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58093210-G-A

173181545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58092814-A-G

173182440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58091637-C-T

173182444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58091633-G-A

http://identifiers.org/hco/4/GRCh38#173182615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#58091516-C-A

173182637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58091508-A-T

173182719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58091490-G-A

173182719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58091490-G-T

173182764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58091480-C-G

173182862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58091390-C-T

173183337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58091109-C-G

173183423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58091029-A-G

173183456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58090996-T-A

173184763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58090876-G-A

173184820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58090820-C-T

173184901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58090738-C-T

173185255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58090424-T-C

173185266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58090413-C-T

173185471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58090206-G-A

173185471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58090206-G-C

173185956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58089708-A-T

173186043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58089633-T-C

173186384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58089143-G-A

173186518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58089008-T-C

173187158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58088449-C-G

173187335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58088289-C-T

173187345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58088284-A-G

173187345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58088284-A-T

173187411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58088172-A-T

173187440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58088142-C-G

173188001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58087573-C-G

173188441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58087048-C-T

173188489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58086995-G-C

http://identifiers.org/hco/4/GRCh38#173188513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58086971-A-C

173189174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58086204-A-T

173189210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58086150-A-G

173189473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58085358-G-A

http://identifiers.org/hco/4/GRCh38#173189859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58084921-A-C

173189859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58084921-A-G

173189895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58084885-T-G

173190006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58084777-T-C

173190030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58084754-G-T

173190566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58083058-C-G

173190778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58082850-C-T

173193120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58080746-G-T

173193483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58080376-C-T

173193731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58080114-T-A

173194370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58079484-G-A

173194370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58079484-G-C

173196062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58077695-C-T

173196994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58077344-A-G

173197112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58077201-G-T

173197118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58077195-G-A

173197118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58077195-G-T

173197183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58077133-A-G

173197232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58077079-A-G

173197299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58077016-G-A

173197435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58076821-A-G

173197700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58076478-A-T

173197722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58076445-A-G

173197731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58076436-C-G

173197952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58076273-C-T

173198160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58075990-C-T

173198320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58075766-G-A

173198320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58075766-G-C

173199889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58073658-A-G

http://identifiers.org/hco/4/GRCh38#173199985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58073571-C-A

173200045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58073511-A-T

173200064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58073497-C-G

173200851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58072726-A-G

173200992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58072582-T-C

173201600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58071924-A-T

173201958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58071022-A-G

173201977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58071003-C-G

173209453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58068736-C-T

173209588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58068646-A-G

173209707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58068526-C-T

173209710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58068523-C-T

173210336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58068218-C-T

173211337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58067692-G-A

173212454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58066682-A-T

173212676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58066475-A-G

173212678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58066473-A-T

173212934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58066251-T-C

173213135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58066079-C-G

173213227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58065986-G-C

173213645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58065588-G-A

http://identifiers.org/hco/4/GRCh38#173213669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58065564-C-A

173213669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58065564-C-T

173214050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58065202-G-A

173214051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58065201-G-A

http://identifiers.org/hco/4/GRCh38#173214278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58064965-C-A

http://identifiers.org/hco/4/GRCh38#173214718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58064536-C-A

173214923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58064335-C-T

173215071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58064193-T-G

173215235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58064022-T-C

173215772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58063865-A-G

173216212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58063771-T-C

173216258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58063727-A-G

173216319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58063669-A-G

173216342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58063642-G-A

173216388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58063593-G-A

173216449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58063539-T-C

173216457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58063531-C-G

173216678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58063323-T-G

173217445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58062584-A-G

173217491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58062538-A-G

173217502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58062527-G-A

173218458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58061532-C-G

173218802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58061181-T-C

173218850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58061067-G-C

173218864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58061053-T-A

173221498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58060581-G-A

173221498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58060581-G-T

173221667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58060335-A-G

http://identifiers.org/hco/4/GRCh38#173223137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58059129-A-C

173223137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58059129-A-G

http://identifiers.org/hco/4/GRCh38#173223186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58059084-A-C

173223217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58059053-T-G

173223224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58059046-A-G

173227909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58056116-C-T

173228235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58055783-G-A

173228296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58055724-G-T

173228325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58055717-C-T

173228336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58055706-T-C

173228338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58055704-A-G

173230348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58055009-A-G

173230466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58054873-G-A

173230558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58054788-G-C

173230698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58054546-G-A

173231087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58054156-A-G

http://identifiers.org/hco/4/GRCh38#173231232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58054014-C-A

173236357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58052819-C-T

173236424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58052757-T-C

173236435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58052746-A-G

http://identifiers.org/hco/4/GRCh38#173237052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58050198-A-C

173237438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58049830-G-A

http://identifiers.org/hco/4/GRCh38#173237488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58049780-C-A

173237583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58049679-T-G

173237787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58049312-T-A

http://identifiers.org/hco/4/GRCh38#173237982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58049120-C-A

173238541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58048574-C-G

173238697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58048420-T-C

173238900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58047896-T-C

173238900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58047896-T-G

173239330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58047420-A-G

173239346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58047404-T-A

173239409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58047340-G-A

173239952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58046799-C-G

173239952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58046799-C-T

http://identifiers.org/hco/4/GRCh38#173240015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58046737-C-A

173240015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58046737-C-G

173240054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58046624-T-A

173240193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58046381-T-A

173240237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58046337-G-A

http://identifiers.org/hco/4/GRCh38#173240349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58046232-A-C

173240390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58046100-A-G

173240390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58046100-A-T

173240408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58046082-G-A

http://identifiers.org/hco/4/GRCh38#173240839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58045491-A-C

173240839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58045491-A-G

173241033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58045301-C-T

173241268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58045236-G-C

173241274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58045230-T-A

173241435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58045091-A-G

173241657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58044592-G-T

173241910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58044288-G-T

173241934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58044282-T-G

http://identifiers.org/hco/4/GRCh38#173242079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58044161-A-C

173242245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58044023-C-T

173242335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58043926-G-A

173242456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58043779-T-C

http://identifiers.org/hco/4/GRCh38#173242485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58043562-A-C

http://identifiers.org/hco/4/GRCh38#173242592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58043395-A-C

173242592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58043395-A-G

173242701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58043295-G-A

173242739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58043259-A-T

173242866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58043136-G-A

173243077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58042750-G-A

173243324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58042552-A-G

173243458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58042421-G-T

173243486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58042405-A-G

173243589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58042306-C-T

173243598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58042297-C-T

173243746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58042147-T-G

173243836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58042065-C-T

173244097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58041829-A-G

173244391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58041503-A-G

173244624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58041285-T-G

173244799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58041114-T-C

173244996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58040937-T-G

173245292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58040663-A-G

http://identifiers.org/hco/4/GRCh38#173246478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58038636-C-A

173246521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58038594-C-T

173246612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58038502-A-G

173246951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58038206-C-T

173247018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58038139-A-G

173247057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58038102-C-T

173247079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58038080-G-C

173247161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58038000-A-G

173247237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58037925-T-C

173247340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58037840-G-T

173247382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58037799-C-T

173247398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58037783-A-G

173247858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58037389-T-G

173247924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58037316-C-T

http://identifiers.org/hco/4/GRCh38#173247944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58037295-C-A

173247944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58037295-C-T

http://identifiers.org/hco/4/GRCh38#173248170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58037069-A-C

173248170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: missense variant
orthologous variants: 58037069-A-G

173248280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: missense variant
orthologous variants: 58036959-C-T

173248325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: synonymous variant
orthologous variants: 58036914-T-C

173248388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: missense variant
orthologous variants: 58036851-G-T

173248522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58036720-G-A

173248524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58036718-A-G

173248562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58036680-A-G

173248628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58036617-T-G

173248648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58036598-G-A

173249529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58035783-C-T

173249749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58035568-A-G

173249889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58035411-G-A

173250011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58035334-G-A

173250011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58035334-G-T

173250620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58034914-C-T

173250723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58034827-A-G

173250733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58034817-G-A

173250734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58034816-T-C

173250810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58034745-C-T

173250970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58034593-T-C

173251027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58034535-G-T

173251031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58034531-T-C

173251031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58034531-T-G

173251178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58034273-C-T

173251287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58034172-G-T

http://identifiers.org/hco/4/GRCh38#173251304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58034155-C-A

173251358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58034105-T-A

173251747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58033843-A-G

173252077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58033245-T-C

173252100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58033223-A-G

173252139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58033186-C-T

173252162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58033163-T-A

173252536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58032840-A-G

173252723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58032676-G-T

173252797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, undefined
orthologous variants: 58032565-G-A

173253380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58032317-G-T

173253508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58032212-G-T

173253524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58032193-G-A

173253524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58032193-G-T

173253565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58032148-G-A

173253582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58032130-T-C

173253841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58031860-A-G

173254245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58031407-C-T

173254921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58030604-T-G

173255065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58030432-A-G

173255065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58030432-A-T

173255138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58030351-G-C

173255439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58030062-A-G

173255450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58030051-C-T

173255453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58030048-A-G

173255638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58029786-C-T

173255657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58029767-A-G

173255683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58029741-C-T

173255809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58029600-A-G

173255847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58029557-C-T

173255856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58029548-T-A

173255971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58029426-T-C

173255979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58029418-T-G

173256201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58029230-C-T

173256305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58029126-T-G

173256410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58029024-G-A

173256410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 58029024-G-C

173256688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58028811-A-G

173256707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58028796-A-G

173256866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58028674-T-C

173256921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58028620-A-G

173257020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 58028523-G-A

173257405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58028191-A-G

173257542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58028051-T-G

173258062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58027516-A-G

173258069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58027509-C-T

173258084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58027494-C-T

173263502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58027137-G-A

173263605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58027025-T-C

173264026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58026672-A-G

173264282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58026530-A-G

173264287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58026525-T-A

173264732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58026171-C-T

173264764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58026141-A-T

173264976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58025938-A-G

173265058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58025863-G-A

173265239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58025684-A-G

173265345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58025560-G-A

173265431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58025483-C-G

173265431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58025483-C-T

173265505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58025416-G-A

173265518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58025410-C-T

173265815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58024478-A-G

173265815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58024478-A-T

http://identifiers.org/hco/4/GRCh38#173265824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58024469-A-C

173265864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58024433-A-G

173265893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58024411-A-G

173265952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58024359-A-T

173266515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58024123-T-C

173266541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58024096-T-C

173267752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58022444-T-C

173267863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58022328-A-G

173267990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58022224-T-G

173267992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58022222-T-A

173267992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58022222-T-C

173268011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58022203-C-T

http://identifiers.org/hco/4/GRCh38#173268034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58022184-A-C

173268156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58022066-T-G

173269477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58020343-A-G

173270284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58019969-A-G

173270548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58019516-A-G

173270554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58019510-A-G

173270813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58019268-C-T

173270960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58019131-A-G

173271023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58019056-T-A

173271110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58018991-C-G

173271638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58018585-G-A

173271638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58018585-G-C

173271638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58018585-G-T

173271655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58018568-C-T

173271756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58018502-C-T

173271843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58018437-T-A

173271850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58018431-A-G

173271998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58018296-T-A

173272053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58018241-G-A

173272135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58018157-T-A

173272143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58018149-C-G

173272381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58017851-T-C

http://identifiers.org/hco/4/GRCh38#173272641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58017446-C-A

173272641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58017446-C-T

173272804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58017294-T-G

173272988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58017134-C-G

173273350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58016795-A-T

173273442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58016708-G-A

173273562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58016584-C-T

173273649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58016502-T-C

173274282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58015885-A-G

173274898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58014482-T-C

173275056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58014337-A-G

173275107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58014281-T-C

173275264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58014158-A-G

http://identifiers.org/hco/4/GRCh38#173275319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58014106-C-A

173275500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58013879-G-A

173275560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58013752-C-G

173275767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58013566-A-G

173275831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58013509-A-G

173275968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58013393-G-A

http://identifiers.org/hco/4/GRCh38#173276417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58012953-C-A

173276417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58012953-C-G

173276715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58012670-G-A

173277078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58011980-A-G

173277107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58011951-T-C

173277340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58011748-G-A

http://identifiers.org/hco/4/GRCh38#173277371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58011725-A-C

173277371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58011725-A-G

173277488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58011597-G-A

173277488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58011597-G-C

173277517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58011569-T-C

173277545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58011541-G-A

173277750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58011203-G-C

173277750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58011203-G-T

173277927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58010947-A-G

173277950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58010924-G-A

173278059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58010838-G-A

http://identifiers.org/hco/4/GRCh38#173278249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58010460-C-A

173278249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58010460-C-T

173278276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58010407-T-C

173278364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58010322-G-A

173278369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58010318-C-T

http://identifiers.org/hco/4/GRCh38#173278460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58010224-C-A

173278630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58010033-T-A

173278672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58009991-G-T

173278746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58009893-T-C

173278894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58009803-G-A

173280394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58008742-A-G

173280394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58008742-A-T

173280488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58008382-C-T

173280653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58008235-G-A

173280653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58008235-G-T

http://identifiers.org/hco/4/GRCh38#173280668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58008220-A-C

173280737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58008155-C-T

http://identifiers.org/hco/4/GRCh38#173280796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58007787-C-A

173291740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005994-T-A

http://identifiers.org/hco/4/GRCh38#173291750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58005984-C-A

173291750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005984-C-T

http://identifiers.org/hco/4/GRCh38#173291763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58005969-C-A

173291819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005925-C-T

173291836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005909-C-T

173291974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005778-T-C

173291990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005766-T-G

http://identifiers.org/hco/4/GRCh38#173292032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58005724-C-A

173292054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005696-G-T

http://identifiers.org/hco/4/GRCh38#173292098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58005652-C-A

173292098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005652-C-T

http://identifiers.org/hco/4/GRCh38#173292244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58005506-A-C

173292244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58005506-A-G

173292244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58005506-A-T

173292299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005451-T-C

173292315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005435-T-A

http://identifiers.org/hco/4/GRCh38#173292317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58005433-A-C

173292414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005346-G-T

173292419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005341-G-T

http://identifiers.org/hco/4/GRCh38#173292426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58005334-A-C

173292426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005334-A-G

173293380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58001442-G-C

173293595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58001209-G-A

http://identifiers.org/hco/4/GRCh38#173293886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#58000770-C-A

173293886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000770-C-T

173293930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000725-C-T

173294173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000535-G-A

173294179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000529-A-T

173294186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000522-A-G

173294265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000435-G-A

173294321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000363-G-A

173294975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57999352-T-C

173294993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57999334-A-T

173295543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57998684-A-G

http://identifiers.org/hco/4/GRCh38#173295549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57998670-A-C

173295562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57998657-T-G

173295602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57998603-T-G

173295605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57998600-G-A

173295812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant
orthologous variants: 57998392-G-A

173295864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57998335-T-C

http://identifiers.org/hco/4/GRCh38#173295887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57998310-C-A

173295976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57998219-T-A

173295976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57998219-T-C

http://identifiers.org/hco/4/GRCh38#173295983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57998212-C-A

173296130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57998100-A-G

173296541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57997602-T-C

173296929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57997215-T-C

173296929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57997215-T-G

173297421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57996815-C-G

173297421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57996815-C-T

173297583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57996259-G-A

173297667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57996180-A-G

http://identifiers.org/hco/4/GRCh38#173297700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57996147-C-A

173297700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57996147-C-T

173298070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57995770-T-C

173298438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57995397-A-G

173298438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57995397-A-T

http://identifiers.org/hco/4/GRCh38#173298487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57995350-A-C

173298497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57995340-C-G

173298497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57995340-C-T

173298577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57995262-A-G

173298849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57994993-A-G

173299048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57994799-G-A

173299304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57994568-A-G

173299323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57994549-C-T

173301236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993953-T-G

173301415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993767-A-G

173301656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993528-G-A

173301656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993528-G-T

173301939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993278-G-A

173301939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993278-G-T

173301991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993226-T-C

173301991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993226-T-G

173302006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993211-G-A

173302006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993211-G-T

173302063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57993153-G-A

http://identifiers.org/hco/4/GRCh38#173302078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57993138-A-C

http://identifiers.org/hco/4/GRCh38#173302281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57992531-C-A

173302281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992531-C-T

173302295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992517-T-C

http://identifiers.org/hco/4/GRCh38#173302315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57992500-C-A

173302315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992500-C-T

173302357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992478-C-G

173302476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992364-G-C

173302824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992120-C-T

173303323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991886-G-C

173303375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991845-A-G

173303453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991769-G-A

173303669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991557-A-G

173303687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991539-T-G

173303729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991495-A-G

173303844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991385-A-G

http://identifiers.org/hco/4/GRCh38#173303881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57991349-C-A

173303881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991349-C-G

173303893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991337-T-A

173303893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991337-T-G

173304136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991093-A-G

http://identifiers.org/hco/4/GRCh38#173304153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57991076-C-A

173304153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991076-C-T

173304165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991064-T-C

http://identifiers.org/hco/4/GRCh38#173304516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57990986-A-C

173304686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57990864-C-T

173304690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57990859-C-T

173305042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57990506-T-G

http://identifiers.org/hco/4/GRCh38#173312703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57990430-A-C

http://identifiers.org/hco/4/GRCh38#173313142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57990316-C-A

173313144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57990314-A-G

173313212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57990266-C-T

173313824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57989970-T-C

173313841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57989948-T-G

173313884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57989905-T-C

http://identifiers.org/hco/4/GRCh38#173313927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57989857-C-A

173313927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57989857-C-T

173314240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57989540-G-A

173314329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57989447-T-C

http://identifiers.org/hco/4/GRCh38#173314592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57989207-A-C

173314702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57989160-T-A

173314925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57988922-T-A

173314977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57988879-A-G

173315017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57988824-A-G

173315172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57988603-G-A

173315209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57988175-G-A

173315328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57988065-G-C

173315347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57988033-G-A

173315485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57987900-A-G

http://identifiers.org/hco/4/GRCh38#173315570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57987824-C-A

173315586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57987808-G-A

173315648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: 57987751-T-G

http://identifiers.org/hco/4/GRCh38#173315823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57987390-C-A

173315926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57987288-C-T

http://identifiers.org/hco/4/GRCh38#173316062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57987153-C-A

173316062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57987153-C-G

173316106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57987099-T-C

173316121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57987084-T-C

173316125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57987080-T-G

173316206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57987013-A-G

173316207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57987012-G-T

http://identifiers.org/hco/4/GRCh38#173316211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57987002-C-A

173316211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57987002-C-G

173316211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57987002-C-T

http://identifiers.org/hco/4/GRCh38#173316364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57986855-C-A

173316418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986797-T-C

173316499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986744-T-A

http://identifiers.org/hco/4/GRCh38#173316613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57986662-C-A

173316639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986632-G-C

173316640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986631-A-G

173316640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986631-A-T

173316654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986607-T-C

173316654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986607-T-G

173316668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986593-G-T

http://identifiers.org/hco/4/GRCh38#173316791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57986434-C-A

173316842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57986391-G-A

173316842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57986391-G-T

173316887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986352-A-G

http://identifiers.org/hco/4/GRCh38#173316980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57986258-C-A

173316980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986258-C-T

173317028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986229-T-C

173317109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986148-T-C

173317231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57986022-C-T

173317279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57985980-G-A

http://identifiers.org/hco/4/GRCh38#173317299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57985965-C-A

http://identifiers.org/hco/4/GRCh38#173317314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57985944-C-A

173317314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57985944-C-G

173317314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57985944-C-T

173317347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57985920-G-T

173317506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57985877-T-C

173317646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57985746-G-A

http://identifiers.org/hco/4/GRCh38#173317777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57985621-C-A

173317788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57985610-A-G

173317880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57985485-T-C

http://identifiers.org/hco/4/GRCh38#173318126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57985109-C-A

173318284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984900-T-C

173318296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984888-T-A

173318296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984888-T-C

173318296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984888-T-G

http://identifiers.org/hco/4/GRCh38#173318356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57984828-A-C

http://identifiers.org/hco/4/GRCh38#173318397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57984784-C-A

173318397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984784-C-G

173318431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 57984762-C-G

173318431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 57984762-C-T

173318563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57984630-T-C

173318563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57984630-T-G

http://identifiers.org/hco/4/GRCh38#173318565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57984628-C-A

173318565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57984628-C-G

173318565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57984628-C-T

173318566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57984627-T-A

173318566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57984627-T-C

173318567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57984626-G-A

173318567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57984626-G-C

173318569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57984624-A-G

173318572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57984621-T-C

173318677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984511-T-C

http://identifiers.org/hco/4/GRCh38#173318770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57984428-C-A

173318770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984428-C-T

173318859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984338-A-G

173318859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984338-A-T

173321058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57980624-C-G

173321167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57980519-G-A

173321224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57980459-A-G

173321560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57979303-T-A

173321560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57979303-T-C

173322414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57978435-A-G

http://identifiers.org/hco/4/GRCh38#173322760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#57978106-A-C

173322958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57977893-G-T

173323019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57977837-A-G

173323508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57977316-T-C

173323627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57977197-T-A

173323647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57977182-A-G

173323871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57976956-A-G