104802130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83066904-T-A

104802614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83067273-G-A

104802618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83067277-G-T

104802669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83067329-A-G

104802768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83067445-C-T

104802849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83067497-A-T

104803123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83067718-A-G

104803128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83067723-G-A

104803147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83067742-T-A

104803168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83067768-T-C

104803168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83067768-T-G

http://identifiers.org/hco/12/GRCh38#104803524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83068201-C-A

104803534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068211-A-T

http://identifiers.org/hco/12/GRCh38#104803543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83068220-C-A

104803550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068227-T-C

104803592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068258-A-G

104803627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068293-G-A

104803627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068293-G-T

http://identifiers.org/hco/12/GRCh38#104803950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83068551-A-C

104803952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068553-A-G

104803952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068553-A-T

104803961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068561-T-G

104804441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068682-C-T

104804502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068799-T-C

104804502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068799-T-G

104804652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068948-G-A

104804652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83068948-G-T

104804746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83069038-G-C

104804746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83069038-G-T

http://identifiers.org/hco/12/GRCh38#104804832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83069114-C-A

104804832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83069114-C-T

104804846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83069128-T-C

104804909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83069192-G-A

104804909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3 prime UTR variant
orthologous variants: 83069192-G-T

104805066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83069346-A-T

104805088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83069367-A-G

104805134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83069411-A-G

104805319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83069596-T-C

104805368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83069645-T-G

104805396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83069658-T-C

104805492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83069745-A-G

http://identifiers.org/hco/12/GRCh38#104809383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83069910-A-C

104809383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83069910-A-T

104814711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83077585-G-C

104814829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83077692-T-C

104814857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83077713-T-C

104814882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83077741-T-G

104815131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83077972-G-A

104815218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83078059-C-G

104815622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83078446-G-C

http://identifiers.org/hco/12/GRCh38#104815909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83078714-A-C

104816060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83078816-G-A

http://identifiers.org/hco/12/GRCh38#104816166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83078914-C-A

104823428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83082147-A-G

http://identifiers.org/hco/12/GRCh38#104831859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83082524-A-C

http://identifiers.org/hco/12/GRCh38#104832059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83082992-A-C

104832059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83082992-A-G

104832070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83083003-A-G

104832241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83083112-C-T

104832264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83083133-T-C

104832338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83083206-A-G

http://identifiers.org/hco/12/GRCh38#104832367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83083233-A-C

104832486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83083328-T-C

http://identifiers.org/hco/12/GRCh38#104832500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83083343-C-A

104832512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83083353-A-G

104832647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83083503-T-G

104832691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83083593-G-A

104832691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83083593-G-T

http://identifiers.org/hco/12/GRCh38#104832741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83083643-C-A

http://identifiers.org/hco/12/GRCh38#104832751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83083653-A-C

104833000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83083971-A-G

104833010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83083981-T-C

104833058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83084019-A-G

104833130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83084087-A-G

104833554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83084409-C-T

104833574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83084441-A-G

104833955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83084663-T-C

104834112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83084803-G-A

104834112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83084803-G-T

http://identifiers.org/hco/12/GRCh38#104834320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83085573-C-A

http://identifiers.org/hco/12/GRCh38#104834725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83086448-C-A

http://identifiers.org/hco/12/GRCh38#104834791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83086514-A-C

104838468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83086902-T-A

104838468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83086902-T-C

104838605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83087018-T-G

http://identifiers.org/hco/12/GRCh38#104839284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83087796-C-A

104843950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83087950-A-G

104844090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83088081-A-G

104844117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83088108-A-G

104844404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83090578-T-C

104844640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83090814-A-G

104844650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83090824-A-G

104844705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83091062-T-C

104844989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83091316-A-G

104845248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83091410-A-G

104845820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83091848-T-C

104845904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: synonymous variant
orthologous variants: 83091936-T-C

104845997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83092029-G-A

104845997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83092029-G-T

104846104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, undefined
orthologous variants: 83092129-T-C

104846104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, undefined
orthologous variants: 83092129-T-G

104846112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83092137-T-C

104846682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83092854-G-C

104846842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83093083-G-A

104846919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83093151-A-G

104846979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83093210-A-G

104847042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83093277-G-C

104847058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83093293-G-A

104850092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83097827-G-C

104850092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83097827-G-T

104850111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83097846-T-C

104850313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83098846-G-A

104850313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83098846-G-T

104850410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83098947-G-T

http://identifiers.org/hco/12/GRCh38#104850780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83100515-A-C

104850960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83100690-G-A

104851066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83100782-A-G

104851718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83102197-G-T

104851778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83102271-T-A

104851778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83102271-T-C

http://identifiers.org/hco/12/GRCh38#104851875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83102328-A-C

104851896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83102348-A-G

104851969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83102392-C-G

104851969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83102392-C-T

104852187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83102602-A-G

104852267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83102657-T-C

104852689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83102983-T-C

104852707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83103001-T-G

104852728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83103020-C-T

104853059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83103337-C-T

104853254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83103641-C-T

104853275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83103663-C-T

104853449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83103811-T-C

104853499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83103881-T-G

104858057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83114481-G-A

104858057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83114481-G-T

104858298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83114714-C-T

104858303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83114719-T-C

104858347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83114764-C-G

104858498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83114909-T-C

104858498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83114909-T-G

104858803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83115255-T-C

104858803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83115255-T-G

104858940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83115382-T-C

104859147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83115573-G-C

104859147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83115573-G-T

104859182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83115645-G-A

104859328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83115782-G-A

104859435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83115873-T-G

104859588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83115991-A-G

104859734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83116119-A-T

104861175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117161-G-A

104861179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117165-G-A

104861179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117165-G-T

104861181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117167-G-A

104861181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117167-G-T

104861223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117194-A-G

104861257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117200-G-T

http://identifiers.org/hco/12/GRCh38#104861272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83117215-C-A

104861272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117215-C-T

104861410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117351-G-A

104861410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117351-G-C

104861420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117361-T-C

http://identifiers.org/hco/12/GRCh38#104861446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83117386-C-A

104861446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117386-C-T

104861511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117465-G-A

104861511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117465-G-C

104861511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83117465-G-T

104861846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83118557-T-C

104861921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83118598-G-C

http://identifiers.org/hco/12/GRCh38#104861978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83118658-C-A

104862022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83118702-G-A

104866563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 83119717-A-G

104868302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83121774-A-G

104868345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83121817-A-G

104868444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83121909-G-A

104868633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83122102-G-A

104868672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83122127-T-C

http://identifiers.org/hco/12/GRCh38#104868818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83122270-C-A

104869210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83122498-C-T

104869375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83122583-C-T

104869429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83122612-T-C

104869487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83122662-G-T

104869490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83122665-C-T

104869510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83122685-A-G

104869577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83122737-A-T

104869592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83122752-C-T

104869900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83122893-C-T

104870078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83123054-G-C

104870156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83123098-T-C

104870278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83123192-A-G

http://identifiers.org/hco/12/GRCh38#104870413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83123310-A-C

http://identifiers.org/hco/12/GRCh38#104870467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83123334-A-C

104870467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83123334-A-G

104870481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83123348-T-C

104870594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83123455-C-T

104870703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83123550-T-C

http://identifiers.org/hco/12/GRCh38#104870711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83123558-A-C

http://identifiers.org/hco/12/GRCh38#104870877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83123701-C-A

104870893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83123716-A-G

104870970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83123795-G-C

http://identifiers.org/hco/12/GRCh38#104871056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83123894-C-A

104871056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83123894-C-T

104871379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83128137-T-C

104871408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83128162-C-T

104871469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83128223-C-T

104871582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83128333-T-G

104871618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83128372-A-G

104871734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83128501-T-A

http://identifiers.org/hco/12/GRCh38#104875965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83129614-C-A

104875965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83129614-C-G

104875965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83129614-C-T

104876129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83129737-T-C

104876151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83129766-G-A

http://identifiers.org/hco/12/GRCh38#104876238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83129853-C-A

104876243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83129858-C-T

104876475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83130052-A-G

http://identifiers.org/hco/12/GRCh38#104876854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83130362-C-A

104877019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83130500-A-G

104877019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83130500-A-T

104877036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83130516-G-A

104877040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83130520-A-G

104877055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83130555-A-G

104877074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83130574-T-A

104877114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83130615-T-C

http://identifiers.org/hco/12/GRCh38#104877245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83130730-C-A

104877306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, undefined
orthologous variants: 83130776-C-T

104877342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, undefined
orthologous variants: 83130812-C-T

104877654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83131293-T-C

104886075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83132815-G-A

104886210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83132946-C-T

104886225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83132961-T-C

104886453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83133178-T-A

104886483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83133206-G-A

http://identifiers.org/hco/12/GRCh38#104886554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83133277-A-C

104886557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83133280-T-A

http://identifiers.org/hco/12/GRCh38#104886565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83133288-C-A

http://identifiers.org/hco/12/GRCh38#104886567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83133290-A-C

http://identifiers.org/hco/12/GRCh38#104886640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83133361-A-C

104886655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83133373-G-C

104886710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83133410-G-T

104886753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83133477-A-G

http://identifiers.org/hco/12/GRCh38#104887336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83135041-A-C

104887346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83135051-G-C

104887381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83135085-G-C

104887472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83135176-A-G

104887684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83135346-T-C

104887759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83135402-G-A

http://identifiers.org/hco/12/GRCh38#104887834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83135453-C-A

104887855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83135475-A-G

104887906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83135525-A-G

http://identifiers.org/hco/12/GRCh38#104887907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83135526-C-A

104888292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83135839-C-G

104888326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83135853-C-G

104888564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83136219-G-A

104888881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83136878-T-A

104888881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83136878-T-C

104889085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: missense variant
orthologous variants: 83137078-T-C

104889087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: missense variant
orthologous variants: 83137080-T-C

104889313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83137296-T-A

104889313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83137296-T-C

104889315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83137298-G-T

104891168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83137707-G-C

104891525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83138056-A-T

104894753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83138476-T-G

104895180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83140123-G-A

104895180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83140123-G-T

104895841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83141326-T-C

104895859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83141339-T-C

104895882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83141363-T-G

104896103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83141634-C-T

104896386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, undefined
orthologous variants: 83142147-A-G

http://identifiers.org/hco/12/GRCh38#104896717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83142446-A-C

http://identifiers.org/hco/12/GRCh38#104904164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83146393-A-C

104906105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83146711-T-C

104909519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83149141-T-C

104909519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83149141-T-G

104909604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83149229-G-A

104909604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83149229-G-T

104911509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83151043-C-T

104928125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: missense variant
orthologous variants: 83152068-T-C

104928125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: missense variant
orthologous variants: 83152068-T-G

104928309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: synonymous variant
orthologous variants: 83152255-T-C

http://identifiers.org/hco/12/GRCh38#104928578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83152523-C-A

http://identifiers.org/hco/12/GRCh38#104928583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83152528-C-A

104928697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 83152656-G-A

104928697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 83152656-G-T

104928945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83153036-T-C

http://identifiers.org/hco/12/GRCh38#104928976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83153067-C-A

104928976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83153067-C-T

104929556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83153976-A-T

104929613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83154024-A-T

104929649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83154046-C-T

http://identifiers.org/hco/12/GRCh38#104929749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83154137-C-A

104929750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83154138-T-A

104929750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83154138-T-C

104929907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83154217-G-C

104929937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83154247-A-T

104938475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83156863-G-A

104938539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83156927-A-G

104941063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83160097-T-C

104941255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83160246-A-G

104941495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83160474-C-T

104944099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83162158-C-T

104944437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83162590-C-T

104944607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83162759-T-C

104944619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83162771-T-A

104948883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83164418-G-A

104949984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83164758-A-G

104951768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83165770-G-C

104951858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83165882-C-T

104951960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83165979-A-G

104952547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83167159-G-A

104952595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83167203-T-C

104953850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83168290-G-C

104953921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83169345-G-A

104953966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83169397-A-T

104954071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83169518-A-G

http://identifiers.org/hco/12/GRCh38#104954109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83169573-C-A

104954291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83169813-C-T

104954387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83169933-C-T

104954593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83170389-T-C

http://identifiers.org/hco/12/GRCh38#104954606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83170399-C-A

104954606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83170399-C-T

104954666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83170453-G-A

104954776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83170561-A-G

104954797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83170581-T-C

104954983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83170767-A-T

104955470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83170896-C-T

104955492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83170918-T-G

104955538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83170964-T-A

104955703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83171111-C-T

104955776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83171169-G-T

104955875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83171268-T-C

104956090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83171627-G-C

104956321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83171810-C-T

104957471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83172802-T-A

104957615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83172944-C-G

104957659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83172989-G-A

104957876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83173159-G-C

104957884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83173166-G-C

http://identifiers.org/hco/12/GRCh38#104957939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83173205-C-A

104957939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83173205-C-T

http://identifiers.org/hco/12/GRCh38#104957983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83173245-C-A

104957983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: 83173245-C-T

104958056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83173264-G-A

104958161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83173296-C-T

104958230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 83173315-C-T

http://identifiers.org/hco/12/GRCh38#104958446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#83173487-C-A

104958588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: intron_variant, splice_donor_variant, undefined
orthologous variants: 83173611-A-T

104958654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 83173633-A-G

http://identifiers.org/hco/12/GRCh38#104958682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#83173661-C-A

104958695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5 prime UTR variant
orthologous variants: 83173674-G-T

104958738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5 prime UTR variant
orthologous variants: 83173713-G-A

104958738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31045
most severe consequence: 5 prime UTR variant
orthologous variants: 83173713-G-T