http://identifiers.org/hco/6/GRCh38#106360742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44024912-C-A

106360742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5 prime UTR variant
orthologous variants: 44024912-C-G

106360742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5 prime UTR variant
orthologous variants: 44024912-C-T

http://identifiers.org/hco/6/GRCh38#106360799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44024860-C-A

106360799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5 prime UTR variant
orthologous variants: 44024860-C-G

106360799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5 prime UTR variant
orthologous variants: 44024860-C-T

106360817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5 prime UTR variant
orthologous variants: 44024842-G-A

106360817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5 prime UTR variant
orthologous variants: 44024842-G-T

106360823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5 prime UTR variant
orthologous variants: 44024836-G-T

106360830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5 prime UTR variant
orthologous variants: 44024829-C-T

http://identifiers.org/hco/6/GRCh38#106360902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44024762-C-A

http://identifiers.org/hco/6/GRCh38#106360954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44024708-C-A

106360954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 44024708-C-T

106361044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense_variant, undefined
orthologous variants: 44024621-G-A

106361044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense_variant, undefined
orthologous variants: 44024621-G-T

106361047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense_variant, undefined
orthologous variants: 44024618-C-T

106361058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: synonymous_variant, undefined
orthologous variants: 44024609-C-G

106361085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44024583-A-G

106361085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44024583-A-T

106361131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44024563-T-C

http://identifiers.org/hco/6/GRCh38#106361132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44024562-C-A

106361362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, undefined
orthologous variants: 44024433-C-T

106361484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44024314-T-C

106361657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44024169-G-A

106361682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44024142-T-C

106363351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44023796-C-G

106363351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44023796-C-T

http://identifiers.org/hco/6/GRCh38#106363398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44023751-A-C

106363398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44023751-A-G

106364355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44022838-G-A

106364355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44022838-G-T

106364444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44022750-T-C

106364579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44022620-C-G

106364655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44022549-G-A

106364695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44022508-G-A

106364976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44022282-G-T

106365176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44022183-C-T

106365487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44021932-C-G

106365608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44021857-T-A

106365761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44021747-T-A

106365776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44021733-A-G

106365799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44021710-G-A

106365799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44021710-G-T

106368359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44019422-A-T

http://identifiers.org/hco/6/GRCh38#106368394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44019386-C-A

106368394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44019386-C-G

http://identifiers.org/hco/6/GRCh38#106368395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44019385-A-C

106368395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44019385-A-T

106368397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44019383-C-T

106368431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44019331-T-C

106369226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44016671-A-G

106371164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44014882-T-C

106371205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44014843-C-T

106371304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44014757-C-G

106371304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44014757-C-T

106371534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44014548-C-T

http://identifiers.org/hco/6/GRCh38#106371539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44014543-A-C

106371545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44014537-G-A

106371552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44014531-C-T

106371553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44014530-G-A

106371739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44014328-A-T

106371749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44014318-G-A

106371749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44014318-G-C

106371857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44014210-T-A

http://identifiers.org/hco/6/GRCh38#106372115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44013983-A-C

106372518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44013694-C-G

106372530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44013682-G-A

106372539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44013672-A-G

106372810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44013258-A-G

106372840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44013228-G-A

106376602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44010934-A-G

106376796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44010753-G-T

106377026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44010576-T-C

106377185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44010426-G-A

106377340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44010293-T-C

106377441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44010203-A-G

106377521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44010142-G-A

http://identifiers.org/hco/6/GRCh38#106377613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44010053-C-A

106377650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44010005-T-A

106377650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44010005-T-G

106377680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44009989-A-T

106377690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44009982-A-G

106377854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44009815-T-C

106380181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44007166-C-G

106380296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44005309-G-A

106380331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44005274-C-T

106380709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44004820-G-A

106380728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44004794-A-G

106380728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44004794-A-T

106380813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44004258-A-G

106380902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44004165-G-A

106381058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44004008-G-T

106381366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44003159-G-A

106381813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44002808-C-T

106381821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44002800-C-T

106381848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44002783-C-T

106382031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, undefined
orthologous variants: 44002644-G-A

106382360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44002309-T-G

106382437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44002239-T-A

106382844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44001594-A-T

106382868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44001505-A-G

106382947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44001438-G-A

106382947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44001438-G-T

106383267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44001202-G-A

106383267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44001202-G-T

106383309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44001159-A-G

106383386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44001083-G-A

106383469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000972-G-A

106383660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000786-C-T

106383796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000665-A-G

106383849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000611-G-T

106383884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000574-T-C

106383886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000572-C-G

http://identifiers.org/hco/6/GRCh38#106383887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44000571-A-C

106383903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000556-T-A

106383904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000555-A-G

http://identifiers.org/hco/6/GRCh38#106383966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#44000390-C-A

106383966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000390-C-G

106383985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000371-C-G

106384021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000349-G-A

106384021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000349-G-C

106384031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000339-T-G

106384118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 44000251-G-A

106387378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43997623-C-T

http://identifiers.org/hco/6/GRCh38#106387478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43997525-C-A

106387478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43997525-C-T

106388687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43997278-C-T

106388770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43997198-T-C

106388919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43996948-C-T

http://identifiers.org/hco/6/GRCh38#106389449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43996273-A-C

106390198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43994689-A-G

106394311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43993446-T-C

106394319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43993438-A-G

106394465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43993202-A-G

106394467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43993200-T-A

106396302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43991534-A-G

106396556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43990569-A-G

106397313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43989659-A-G

106397648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43989345-C-T

106397838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43989181-C-T

106397865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43989157-A-G

106397865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43989157-A-T

106398098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43989013-T-C

106398728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43988595-G-A

106399034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43988369-C-G

106399310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43988062-C-T

106399339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43988033-T-C

106399428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43987951-A-G

106403906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43987552-A-G

106403932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43987526-C-T

106403939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43987519-G-C

106404135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43987384-C-T

106404300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43987221-G-A

106404305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43987217-T-C

106411025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43986974-A-T

106416210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43981944-C-T

106416213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43981941-T-C

http://identifiers.org/hco/6/GRCh38#106416229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43981925-C-A

106416229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43981925-C-T

106416297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43981805-T-C

http://identifiers.org/hco/6/GRCh38#106416356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43981745-A-C

106416356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43981745-A-G

http://identifiers.org/hco/6/GRCh38#106416484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43981614-A-C

106416801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43981264-A-G

106418616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43980786-A-T

106418644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43980755-A-G

106418661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43980738-A-G

http://identifiers.org/hco/6/GRCh38#106420666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43979050-A-C

106420666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43979050-A-G

106420675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43979041-G-T

http://identifiers.org/hco/6/GRCh38#106421529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43977425-C-A

106421550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43977404-G-C

106421580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43977380-G-A

106421580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43977380-G-C

106421603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43977356-T-C

106422938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43974952-A-G

106422977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43974926-T-C

106424209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43973801-G-A

106424222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43973788-T-C

106428610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43970551-C-T

106428644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43970516-A-G

106428860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43970324-C-T

106429235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43969551-T-C

106429246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43969526-A-G

106429524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43969231-A-G

106429833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43969011-G-T

106429883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43968982-C-G

106431405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43961142-A-G

106431543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43961093-A-G

106431556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43961080-T-A

106431657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43960750-A-G

106431676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43960731-T-C

106431677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43960730-G-A

106431692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43960717-T-C

106431764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43960643-G-C

106431889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43960552-G-A

106432489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43960001-A-G

106432651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43959815-G-A

106432815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43959654-A-G

106432815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43959654-A-T

106433218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43959191-G-A

106433309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43959101-T-C

106435483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43957630-T-G

http://identifiers.org/hco/6/GRCh38#106435855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43957562-C-A

106435855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43957562-C-T

http://identifiers.org/hco/6/GRCh38#106435909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43957503-A-C

106436221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43957165-G-A

106436221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43957165-G-C

106436249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43957137-C-T

106436267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43957120-G-A

106439099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43956373-G-A

106439544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43955382-G-A

106439544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43955382-G-C

106439599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43955334-C-T

http://identifiers.org/hco/6/GRCh38#106439681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43955253-C-A

106439733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43955191-G-A

106440132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43954861-C-T

106440245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43954734-T-C

106440545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43954544-G-C

106440617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43954470-A-G

http://identifiers.org/hco/6/GRCh38#106440787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43954304-C-A

106441043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43953948-G-A

106441409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43953277-A-G

106441585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43953098-A-G

106441607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43953076-T-C

106441860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43952692-A-T

106442081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: -G-A

106442328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43951554-G-A

106442587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43950942-T-C

106442690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43950847-C-T

106442721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43950816-G-C

106442898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43950650-G-A

106443222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43950428-A-G

106443540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43949743-C-T

106443687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43949610-C-T

http://identifiers.org/hco/6/GRCh38#106444138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43949276-C-A

106444440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43949014-G-C

106445247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, undefined
orthologous variants: 43948417-T-G

106445419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43948287-G-A

106445419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43948287-G-T

http://identifiers.org/hco/6/GRCh38#106445596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43948186-A-C

106445936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43947858-G-A

106445952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43947842-T-C

106446069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43947717-T-C

106446069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43947717-T-G

106446090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43947696-G-A

106446114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43947666-G-T

106446302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43947488-G-A

106446331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43947459-A-G

106446772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43947062-C-G

106446786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43947048-A-G

106446869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43946970-T-C

106446909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43946936-G-A

106446967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43946869-T-C

106446968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43946868-T-C

106448018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43945649-A-G

106448190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43945441-A-G

106448276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43945358-C-G

106448324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43945317-A-G

106448563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43945079-A-T

106448689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43944952-A-G

106448772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43944878-G-A

106448775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43944875-T-C

106449215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43944439-G-A

http://identifiers.org/hco/6/GRCh38#106449242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43944419-C-A

106449242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43944419-C-T

106449245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43944416-A-G

http://identifiers.org/hco/6/GRCh38#106449292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43944377-C-A

106449628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43944167-C-T

106449663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43944134-T-C

106449671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43944126-A-G

106449841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43943959-A-G

http://identifiers.org/hco/6/GRCh38#106450127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43943557-A-C

106450158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43943536-C-T

106450180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43943516-T-C

http://identifiers.org/hco/6/GRCh38#106450218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43943479-A-C

http://identifiers.org/hco/6/GRCh38#106450253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43943443-C-A

106450384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43943321-C-T

http://identifiers.org/hco/6/GRCh38#106450467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43943239-A-C

106450568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43943138-T-A

106450839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43942879-A-G

106451352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43942109-G-A

106451352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43942109-G-C

106451352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43942109-G-T

http://identifiers.org/hco/6/GRCh38#106451359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43942102-A-C

106451359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43942102-A-G

106451359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43942102-A-T

106451418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43942046-A-G

106451418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43942046-A-T

http://identifiers.org/hco/6/GRCh38#106451422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43942042-A-C

106451460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43942007-T-A

http://identifiers.org/hco/6/GRCh38#106451526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#43941949-C-A

106451526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43941949-C-G

106451526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43941949-C-T

http://identifiers.org/hco/6/GRCh38#106451528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#43941947-A-C

106451528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43941947-A-G

106451528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43941947-A-T

http://identifiers.org/hco/6/GRCh38#106451537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43941938-C-A

106451537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43941938-C-T

http://identifiers.org/hco/6/GRCh38#106451552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43941923-C-A

106451552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43941923-C-G

106451552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43941923-C-T

http://identifiers.org/hco/6/GRCh38#106451916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43941462-C-A

106451916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43941462-C-G

106452119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43941282-G-A

106452688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43940867-T-C

http://identifiers.org/hco/6/GRCh38#106452848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43940695-C-A

106452896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43940655-G-A

106452908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43940642-A-T

106452995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43940560-A-G

106453102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43940349-C-T

106453285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43940128-A-G

106453312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43940105-T-C

106453448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43939958-C-G

106453506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43939890-A-T

106453508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43939888-T-C

106453724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43939692-G-T

106459009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43937376-G-A

http://identifiers.org/hco/6/GRCh38#106461103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43935250-A-C

106461988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43934439-A-G

106462488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43934223-G-T

106463444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43933360-C-G

106463483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43933319-T-G

106463553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43933257-T-C

106463625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43933205-T-G

106463818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43933042-T-G

106463884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43932982-G-A

106463884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43932982-G-C

106464357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43932405-T-G

106464364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43932398-G-A

106464461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43932340-T-C

106464461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43932340-T-G

106465077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43931822-C-T

106465411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43931441-G-A

106465448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43931413-T-C

106466309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43930365-T-C

106466437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43929816-T-C

106466437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43929816-T-G

106466516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43929725-G-A

106466912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43929363-G-C

106467017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43929256-G-A

106467038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43929237-A-T

106467078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43929198-T-G

106468025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43928680-G-T

106468026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43928679-T-G

106468140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43928578-A-G

106468173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43928546-A-T

106468281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43928283-G-A

106468281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43928283-G-C

106468314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43928253-T-A

106469617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43927006-T-C

106469646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43926977-C-T

106469693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43926918-G-A

http://identifiers.org/hco/6/GRCh38#106470971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43926194-A-C

106470976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43926189-G-A

106471066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43926078-T-G

http://identifiers.org/hco/6/GRCh38#106471129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43926017-C-A

106471129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43926017-C-G

106472384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43924631-T-C

http://identifiers.org/hco/6/GRCh38#106472868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43924288-C-A

106472868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43924288-C-T

106473129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43924104-G-A

106473748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43920230-C-G

106473749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43920229-T-A

106474075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43919896-C-T

106475185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43916168-A-G

106475307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43916052-T-C

106475324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43916035-G-A

106476224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43915662-C-T

http://identifiers.org/hco/6/GRCh38#106476286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43915572-C-A

106476668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43915250-C-G

http://identifiers.org/hco/6/GRCh38#106476703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43915220-C-A

106476746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43915146-T-C

106476833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43915086-A-T

106477005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43914953-C-T

106477022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43914928-T-C

106477106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43914839-C-T

106477239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43914766-T-C

106477541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43914519-G-A

106477671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43914396-G-A

106477950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43914120-G-A

106478229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43913880-A-T

106479246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43908936-G-A

106480061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43908087-T-C

106480061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43908087-T-G

106480066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43908082-C-T

106480084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43908064-G-A

106480084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43908064-G-T

106480223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43907916-G-A

106480250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43907889-G-C

106481256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43907537-G-A

106481256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43907537-G-T

106481771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43907047-T-C

106481846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43906969-T-C

http://identifiers.org/hco/6/GRCh38#106491750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43900915-C-A

106491877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43900786-A-G

106492128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43900574-G-A

106492157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43900546-A-G

106492229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43900474-A-G

106492249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43900456-A-G

106494243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43899312-G-C

106494245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43899310-A-G

106494409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43899142-T-A

106494410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43899141-A-T

106494533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43899033-T-A

106494591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43898971-T-C

106494692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43898799-T-A

106494802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43898687-C-T

106494986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43898509-A-G

106495192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43898262-G-A

106495387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43898113-G-A

106495387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43898113-G-C

106495505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897990-T-C

106495514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897981-T-C

106495537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897959-G-T

106495593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897909-T-A

http://identifiers.org/hco/6/GRCh38#106495594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43897908-A-C

106495594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897908-A-G

106495662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897847-T-G

106495686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897829-A-G

http://identifiers.org/hco/6/GRCh38#106495845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43897702-C-A

106495845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897702-C-T

106495902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897648-A-G

106496042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897522-T-C

106496078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897488-T-A

106496298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897256-C-T

106496359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43897179-T-C

106497196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43896111-G-A

http://identifiers.org/hco/6/GRCh38#106497261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43896009-A-C

106497530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43895817-G-A

106497584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43895761-T-C

http://identifiers.org/hco/6/GRCh38#106497785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43895574-A-C

106497785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43895574-A-G

http://identifiers.org/hco/6/GRCh38#106498151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43895344-C-A

106498151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43895344-C-T

106498351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43895142-T-C

106498516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893513-A-G

http://identifiers.org/hco/6/GRCh38#106498564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43893465-C-A

106498899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893167-G-C

106498899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893167-G-T

106501299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

106502574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43890091-C-T

106503273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43889314-A-G

106503471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43889096-A-G

106503578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43888996-G-A

106503982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43887697-G-A

106504026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43887655-T-A

106504026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43887655-T-G

106504027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43887654-T-A

106504027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43887654-T-G

http://identifiers.org/hco/6/GRCh38#106504056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43887645-C-A

106504056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43887645-C-T

106504112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43887596-G-T

106504313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43887418-C-T

106504348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43887383-G-A

106504348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43887383-G-T

106504519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43887067-A-G

106504522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43887064-C-T

106504767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43886879-T-C

106504893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43886760-A-G

106505157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43886607-C-T

106505349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43886390-T-C

106505799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43885975-G-A

http://identifiers.org/hco/6/GRCh38#106505814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43885947-C-A

106505977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43885795-G-A

106506318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43885453-C-T

106506325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43885446-C-T

106507138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43885037-C-T

http://identifiers.org/hco/6/GRCh38#106507494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43884758-A-C

http://identifiers.org/hco/6/GRCh38#106507500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43884752-C-A

106507500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43884752-C-G

106507517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43884735-G-T

106507747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43884540-A-G

106507833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43884457-G-A

106507849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43884452-G-A

106508611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43883348-G-A

106508936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43883155-A-G

106508936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43883155-A-T

106509046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43883047-C-T

106509082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43883012-C-G

http://identifiers.org/hco/6/GRCh38#106509505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43882721-C-A

106509505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43882721-C-T

106510065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43882221-G-A

106510075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43882207-C-T

106511352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43880960-G-A

106511352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43880960-G-T

106511355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43880957-G-C

106511379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43880936-G-A

106511531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43880783-A-T

106511645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: synonymous variant
orthologous variants: 43880690-G-A

106511706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43880641-C-G

106511714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43880633-G-C

http://identifiers.org/hco/6/GRCh38#106511715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43880632-A-C

106511715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43880632-A-T

http://identifiers.org/hco/6/GRCh38#106511836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43880517-C-A

http://identifiers.org/hco/6/GRCh38#106511866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43880487-C-A

106511866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 43880487-C-T

http://identifiers.org/hco/6/GRCh38#106511903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43880447-C-A

http://identifiers.org/hco/6/GRCh38#106511928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43880422-C-A

106512098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 43880261-G-A

http://identifiers.org/hco/6/GRCh38#106512125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43880255-C-A

106512125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 43880255-C-G

106512127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 43880253-A-T

106512166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 43880217-G-A

106512214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 43880190-C-G

106512304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 43880100-T-C

http://identifiers.org/hco/6/GRCh38#106512451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43879953-A-C

106512451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43879953-A-T

106512453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43879951-G-A

106512453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43879951-G-C

106512567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43879837-C-T

106512622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43879782-G-A

106512622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43879782-G-C

http://identifiers.org/hco/6/GRCh38#106512885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43879555-C-A

106512885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43879555-C-G

106512910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43879530-G-A

106512910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43879530-G-C

106512910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43879530-G-T

106512915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43879525-G-A

http://identifiers.org/hco/6/GRCh38#106513049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43879412-C-A

106513049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43879412-C-T

106513067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43879402-G-A

106513067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43879402-G-T

106513090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43879391-G-C

106513090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43879391-G-T

106513643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43878926-T-C

106514056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43878687-C-T

106514266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43878515-A-G

106514270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43878511-T-C

106514593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43878212-G-A

106514998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43877825-G-A

106515301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43877323-T-C

106515497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43877136-T-A

106517623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43876574-C-T

106518018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43876164-A-G

http://identifiers.org/hco/6/GRCh38#106519132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43875340-C-A

106519435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: synonymous variant
orthologous variants: 43875037-C-T

106519516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874947-G-A

106519552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874911-A-G

106519698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: synonymous variant
orthologous variants: 43874765-T-C

http://identifiers.org/hco/6/GRCh38#106519743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43874720-A-C

106519904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874565-G-A

106519978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874494-C-T

106519979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874493-C-T

106520005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874464-A-G

106520006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874463-C-T

106520007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: synonymous variant
orthologous variants: 43874462-C-T

106520008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874461-C-T

106520017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874452-T-A

http://identifiers.org/hco/6/GRCh38#106520039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43874430-C-A

106520039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874430-C-T

106520095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874374-C-T

106520197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874272-G-A

106520197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874272-G-T

106520218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874251-C-G

106520218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874251-C-T

http://identifiers.org/hco/6/GRCh38#106520273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43874190-C-A

106520273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874190-C-G

106520273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874190-C-T

106520300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874163-C-T

106520390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874082-C-T

106520438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43874034-T-C

106520439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: synonymous variant
orthologous variants: 43874033-T-C

106520489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43873986-G-A

106520591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43873884-C-G

http://identifiers.org/hco/6/GRCh38#106520777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43873698-A-C

106520777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43873698-A-G

http://identifiers.org/hco/6/GRCh38#106520872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43873603-A-C

106520872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43873603-A-G

106520893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43873582-A-T

106521148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43873327-T-C

106521151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43873324-A-G

106521151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43873324-A-T

106521168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: synonymous variant
orthologous variants: 43873307-A-G

http://identifiers.org/hco/6/GRCh38#106521352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43873147-C-A

106521352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43873147-C-T

106521358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43873141-T-C

106521538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43872974-T-C

106522399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43872343-T-C

106522528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43872251-G-A

106522916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43871293-G-A

106523183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43871081-A-G

106523234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43871008-G-T

106523387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43870814-C-G

106523595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43870240-A-G

106524234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43869922-T-G

106524713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43869206-G-A

106524999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43868833-T-A

106525061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43868769-T-A

http://identifiers.org/hco/6/GRCh38#106525062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43868768-C-A

106525062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43868768-C-G

106525062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43868768-C-T

106525086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43868746-A-T

106525195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43868638-T-C

106525245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43868590-C-T

http://identifiers.org/hco/6/GRCh38#106525307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43868528-A-C

106525376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43868459-G-T

106525410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43868417-T-G

106525571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43867718-T-C

106525996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43866524-A-G

106526185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43866140-G-A

http://identifiers.org/hco/6/GRCh38#106527074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43865432-A-C

106527219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43865309-T-A

http://identifiers.org/hco/6/GRCh38#106527309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43865243-A-C

106527309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43865243-A-G

106527338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: synonymous variant
orthologous variants: 43865214-G-A

106527338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: synonymous variant
orthologous variants: 43865214-G-T

106527364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43865188-A-G

106527459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43865099-C-T

106527550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43865011-G-A

106527550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43865011-G-T

106527585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43864972-T-A

106527585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43864972-T-C

106527585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43864972-T-G

106527644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43864912-A-T

106527723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43864835-T-C

106527765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43864797-G-C

106528297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43863485-C-T

106528331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43863452-T-C

106528577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43863182-A-G

106528689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43863073-A-G

http://identifiers.org/hco/6/GRCh38#106528756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43863026-C-A

http://identifiers.org/hco/6/GRCh38#106530081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43862492-C-A

106530081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43862492-C-T

106530087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43862486-G-C

106530087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43862486-G-T

106530093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43862480-T-A

106530093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43862480-T-C

106530354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43862206-T-G

106530359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43862189-T-G

http://identifiers.org/hco/6/GRCh38#106530369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43862179-A-C

106530553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43861999-A-G

106530571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43861975-T-C

http://identifiers.org/hco/6/GRCh38#106530918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43861620-A-C

106530922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43861613-A-G

106530979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43861135-T-C

106530993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43861121-T-C

106531025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43861093-T-C

106531076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43861042-G-A

106531090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43861028-A-G

106531130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43860980-T-A

106531158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43860954-A-G

106531222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43860887-A-G

106531237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43860872-G-A

106531479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43860646-C-T

http://identifiers.org/hco/6/GRCh38#106533689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43859994-A-C

106533689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43859994-A-G

http://identifiers.org/hco/6/GRCh38#106533700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43859983-C-A

106533817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43859872-G-A

http://identifiers.org/hco/6/GRCh38#106534599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43859131-C-A

106534599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43859131-C-G

106534751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43858985-G-A

106534764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43858972-C-G

106534997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43858814-G-A

http://identifiers.org/hco/6/GRCh38#106535240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43858570-A-C

106537747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43856849-C-T

106537805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43856787-A-G

106538122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43856494-A-G

106538388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43856268-A-T

106538411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43856246-G-A

106538414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43856243-A-G

106538414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43856243-A-T

106538627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43856052-C-T

106538647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43856041-C-T

106538663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43856027-C-T

http://identifiers.org/hco/6/GRCh38#106539306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43855701-C-A

106539308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43855699-G-A

106539308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43855699-G-C

106539886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43855179-G-A

106539934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43855132-A-T

106540189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43854569-C-T

106540336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43854424-C-T

106540744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43853922-T-C

106540999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43853682-T-G

http://identifiers.org/hco/6/GRCh38#106541008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43853673-C-A

106541090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43853616-A-G

106541099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43853607-T-C

106541170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43853524-C-G

106541173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43853521-G-A

106541211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43853433-T-A

http://identifiers.org/hco/6/GRCh38#106541212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43853432-C-A

106541212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43853432-C-T

106541244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, missense_variant
orthologous variants: 43853395-G-T

http://identifiers.org/hco/6/GRCh38#106541282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43853341-C-A

106541295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 43853315-A-G

106541319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43853291-T-C

106541319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43853291-T-G

106541376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43853211-T-A

106541376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43853211-T-C

106541393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43853186-G-C

106541403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43853180-A-G

106541414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43853004-C-G

106541414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43853004-C-T

http://identifiers.org/hco/6/GRCh38#106541450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43852970-C-A

106541452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43852968-A-G

106541700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43852666-A-G

106541907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43852522-T-C

106541913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43852516-T-C

http://identifiers.org/hco/6/GRCh38#106543101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43851499-C-A

106543101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43851499-C-T

106543146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43851419-C-T

106543172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43851394-G-A

106543288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43851307-G-A

106543288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43851307-G-C

106543288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43851307-G-T

106543327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43851280-G-T

106543538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: synonymous variant
orthologous variants: 43851080-G-A

106543538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: synonymous variant
orthologous variants: 43851080-G-T

106543594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43851024-G-A

106543594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43851024-G-C

106543594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43851024-G-T

106543668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43850955-C-T

106543702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43850924-G-C

106544160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43850688-A-G

106544228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43850602-C-T

106544338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43850337-T-A

http://identifiers.org/hco/6/GRCh38#106544341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43850280-C-A

106544346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43850275-A-T

106544365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43850244-T-C

106544450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43850152-T-C

106544539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43850041-A-G

106544590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43849995-C-T

http://identifiers.org/hco/6/GRCh38#106544724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43849861-A-C

http://identifiers.org/hco/6/GRCh38#106544763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43849822-A-C

106544763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43849822-A-G

106544763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43849822-A-T

106544775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43849810-T-G

106544887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43849698-A-G

http://identifiers.org/hco/6/GRCh38#106545008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43849580-C-A

http://identifiers.org/hco/6/GRCh38#106545013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43849573-A-C

http://identifiers.org/hco/6/GRCh38#106545040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43849551-A-C

106545040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43849551-A-T

106545057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43849534-T-C

106545065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43849526-T-C

106545177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43849420-A-G

106545202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43849398-A-G

106545264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43849371-A-G

106545388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43849236-G-A

106545980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43848834-C-T

http://identifiers.org/hco/6/GRCh38#106546205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43848670-A-C

106546349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43848566-T-C

106546462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43848478-T-A

106546577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43848421-C-T

106546757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43848270-G-A

http://identifiers.org/hco/6/GRCh38#106547016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43848066-C-A

106547578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43847025-C-G

http://identifiers.org/hco/6/GRCh38#106547928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43846350-C-A

106547951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43846326-G-A

106547963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43846314-A-G

106547979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43846298-G-A

106547999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43846141-T-C

106548481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43845764-T-C

106548545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43845697-T-C

106550212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43844791-G-C

106550450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43844601-C-G

106550541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43844527-G-A

106550632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43844450-T-C

106550720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43844383-T-C

http://identifiers.org/hco/6/GRCh38#106551726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43843920-C-A

106551726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43843920-C-T

106551781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43843869-A-G

http://identifiers.org/hco/6/GRCh38#106551783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43843867-A-C

106551783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43843867-A-T

106552009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43843657-T-G

106552019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43843647-T-G

106552068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43843604-T-C

106552083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43843590-G-A

106552099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43843574-A-T

106552245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43843439-A-G

106552627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43843380-A-T

http://identifiers.org/hco/6/GRCh38#106553094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43842950-A-C

106553169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43842876-T-C

http://identifiers.org/hco/6/GRCh38#106553341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43842713-C-A

http://identifiers.org/hco/6/GRCh38#106553581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43842283-A-C

106553581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43842283-A-G

106553581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43842283-A-T

106553653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43842216-G-A

106553653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43842216-G-T

106553685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43842186-G-A

106553685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43842186-G-T

106555689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43840770-A-G

106555698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43840761-A-G

106555698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43840761-A-T

106555717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43840742-G-A

106555717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43840742-G-T

106555745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43840720-G-A

106555745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43840720-G-T

106555930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43840545-A-T

106556535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43839502-C-T

106557767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43838351-T-C

106557981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43838194-A-G

106558171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43837913-G-C

106558257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43837803-C-T

http://identifiers.org/hco/6/GRCh38#106558405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43837648-C-A

106558405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43837648-C-T

106558417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43837619-A-T

106558418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43837618-T-A

106558418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43837618-T-C

106558440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43837595-T-A

106558452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43837585-T-C

106558454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43837583-A-G

106558631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43837417-T-C

106558658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43837390-G-C

106558658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43837390-G-T

106560121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43835931-G-C

106560272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43835800-G-A

106560864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43834870-G-A

106560864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43834870-G-T

106561016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834723-A-G

106561025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834714-A-G

106561076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834678-T-C

106561143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834604-C-T

106561166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834582-G-A

106561217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834525-G-C

106561217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834525-G-T

106561224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834518-G-A

106561224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834518-G-C

106561224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834518-G-T

106561231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834511-G-T

106561249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834491-T-C

106561249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834491-T-G

http://identifiers.org/hco/6/GRCh38#106561254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43834486-C-A

106561272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834468-A-T

http://identifiers.org/hco/6/GRCh38#106561296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43834447-C-A

106561306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834437-T-A

106561306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834437-T-G

106561319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834423-C-T

106561325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834417-G-A

106561375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: 43834367-A-G

106561552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43834217-T-C

106563308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43833381-G-C

106563935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43832634-C-T

106566731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43830069-A-G

106566757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43830045-A-G

106566767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43830035-G-T

106566896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43829971-T-C

106567470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43828823-A-G

106567648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43828679-A-G

106567924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43828439-C-T

106568067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43828295-G-A

106568147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43828219-A-T

106568213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43828158-A-G

106568436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43827984-G-T

106568439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: intron variant
orthologous variants: 43827981-A-T

http://identifiers.org/hco/6/GRCh38#106568477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43827946-A-C

http://identifiers.org/hco/6/GRCh38#106568707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43827748-C-A

106568707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43827748-C-T

106568786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43827681-G-A

106568786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43827681-G-T

106568911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43827567-G-A

106568911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43827567-G-T

http://identifiers.org/hco/6/GRCh38#106569548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43827271-C-A

106569583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43827241-T-A

106569583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43827241-T-C

106569757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43827100-G-A

106569757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43827100-G-T

106569836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43827061-T-C

106569979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43827003-G-T

http://identifiers.org/hco/6/GRCh38#106570061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43826933-C-A

106570105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43826911-T-C

106570254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43826795-T-C

106570324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43826754-T-C

106570447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43826632-C-T

106570541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43826578-A-G

http://identifiers.org/hco/6/GRCh38#106570592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43826544-C-A

106570643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43826526-G-T

106570681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43826487-A-T

http://identifiers.org/hco/6/GRCh38#106570705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43826463-C-A

106570705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43826463-C-T

106570856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43826000-G-T

106570921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 356
most severe consequence: 3 prime UTR variant
orthologous variants: 43825928-G-T