98794122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 3 prime UTR variant
orthologous variants: 37651037-C-T

98794246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 3 prime UTR variant
orthologous variants: 37651075-T-C

http://identifiers.org/hco/2/GRCh38#98794247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37651076-C-A

98794376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 3 prime UTR variant
orthologous variants: 37651182-T-G

98794727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37651527-C-T

98794761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37651560-G-A

98794761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37651560-G-T

98794781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37651580-G-A

98794781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37651580-G-C

98794781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37651580-G-T

http://identifiers.org/hco/2/GRCh38#98794804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37651603-C-A

98794804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37651603-C-T

98794820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37651616-T-C

98794849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37651645-T-C

http://identifiers.org/hco/2/GRCh38#98794949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37651743-A-C

98794955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37651757-C-T

http://identifiers.org/hco/2/GRCh38#98795023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37651810-C-A

http://identifiers.org/hco/2/GRCh38#98795030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37651817-C-A

98795340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37651949-T-C

98795661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652160-T-A

98796111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652409-A-G

http://identifiers.org/hco/2/GRCh38#98796241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#37652539-A-C

98796241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous_variant, undefined
orthologous variants: 37652539-A-G

98796274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, undefined
orthologous variants: 37652572-C-T

98796283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, undefined
orthologous variants: 37652584-C-G

98796283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, undefined
orthologous variants: 37652584-C-T

98796284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, undefined
orthologous variants: 37652585-A-G

98796293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, undefined
orthologous variants: 37652596-A-G

98796294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, undefined
orthologous variants: 37652597-G-T

98796313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652613-G-C

98796316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652616-G-A

98796316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652616-G-T

98796325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, undefined
orthologous variants: 37652623-T-C

http://identifiers.org/hco/2/GRCh38#98796340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37652638-C-A

98796340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652638-C-G

98796340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652638-C-T

98796366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652665-T-A

98796366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652665-T-C

98796376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652675-G-A

98796376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652675-G-C

98796376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652675-G-T

98796450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652745-T-C

98796536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652831-T-C

98796584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, undefined
orthologous variants: 37652876-T-C

98796689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652974-C-T

98796715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37652999-C-T

98796938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37653182-G-A

98796994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37653238-T-G

98797107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37653325-C-T

http://identifiers.org/hco/2/GRCh38#98797207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37653410-C-A

98797228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37653420-A-G

98797233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37653425-A-G

98797233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37653425-A-T

98797253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37653449-C-T

98797275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37653499-T-C

98797518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37653730-T-C

http://identifiers.org/hco/2/GRCh38#98797533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37653745-C-A

98797533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37653745-C-G

98797533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37653745-C-T

98797558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37653777-A-G

http://identifiers.org/hco/2/GRCh38#98797618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37653838-C-A

98797618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37653838-C-G

98797618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37653838-C-T

98797627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37653855-T-C

98797759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37654044-T-C

98800963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37655106-G-A

98802479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37656541-A-G

http://identifiers.org/hco/2/GRCh38#98802513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37656567-C-A

98802833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37656884-G-T

98803920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37657716-G-A

98804270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37658009-C-T

98804332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37658061-C-T

98804416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37658140-C-T

98804441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37658165-G-C

http://identifiers.org/hco/2/GRCh38#98805718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#37658703-C-A

98805769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, undefined
orthologous variants: 37658752-C-T

http://identifiers.org/hco/2/GRCh38#98810251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37659876-A-C

98810394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37660011-G-A

98819740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37661565-G-C

http://identifiers.org/hco/2/GRCh38#98819790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37661615-C-A

http://identifiers.org/hco/2/GRCh38#98819791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37661616-A-C

98820143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37661685-G-T

98821075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37662272-A-G

http://identifiers.org/hco/2/GRCh38#98821188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37662392-A-C

98821894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37662873-G-C

98821894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37662873-G-T

http://identifiers.org/hco/2/GRCh38#98821975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37662972-C-A

98821975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37662972-C-T

98822005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37663002-G-A

98822083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37663080-G-A

98822083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37663080-G-C

98822083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37663080-G-T

98822107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37663104-G-A

98822107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37663104-G-T

98822140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37663140-G-A

98822140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37663140-G-C

98822140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37663140-G-T

98822203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37663203-G-A

98822203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37663203-G-T

http://identifiers.org/hco/2/GRCh38#98822468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#37663435-C-A

98822468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, undefined
orthologous variants: 37663435-C-G

98822468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, undefined
orthologous variants: 37663435-C-T

98822497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous_variant, undefined
orthologous variants: 37663479-T-C

http://identifiers.org/hco/2/GRCh38#98822514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#37663496-C-A

98822514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, undefined
orthologous variants: 37663496-C-T

http://identifiers.org/hco/2/GRCh38#98822530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#37663512-C-A

98822530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous_variant, undefined
orthologous variants: 37663512-C-T

98822575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37663563-G-A

98822575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37663563-G-C

98822575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37663563-G-T

http://identifiers.org/hco/2/GRCh38#98822590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37663575-C-A

98822590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37663575-C-T

98822603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37663588-G-A

98822603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37663588-G-T

http://identifiers.org/hco/2/GRCh38#98822662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37663644-C-A

98822662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37663644-C-T

98822677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37663659-T-A

98822677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37663659-T-C

http://identifiers.org/hco/2/GRCh38#98822691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37663673-C-A

98822691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37663673-C-T

98822700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37663682-G-A

98822700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37663682-G-T

98822746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous_variant, undefined
orthologous variants: 37663706-G-A

98822746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous_variant, undefined
orthologous variants: 37663706-G-T

98822845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37663803-G-A

98822845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37663803-G-C

98822845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37663803-G-T

98823038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37664650-G-A

98823038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37664650-G-T

http://identifiers.org/hco/2/GRCh38#98823049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37664661-C-A

98823049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37664661-C-G

98823049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37664661-C-T

98823050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37664662-T-A

98823050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37664662-T-C

98823050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37664662-T-G

http://identifiers.org/hco/2/GRCh38#98823051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#37664663-C-A

98823051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37664663-C-G

98823051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37664663-C-T

http://identifiers.org/hco/2/GRCh38#98823081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37664693-C-A

98823081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37664693-C-T

98823100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous_variant, undefined
orthologous variants: 37664712-C-T

http://identifiers.org/hco/2/GRCh38#98823123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#37664735-C-A

98823123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, undefined
orthologous variants: 37664735-C-T

http://identifiers.org/hco/2/GRCh38#98823163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37664775-C-A

98823163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37664775-C-T

98823164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37664776-T-C

http://identifiers.org/hco/2/GRCh38#98823168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#37664780-C-A

98823168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37664780-C-G

98823168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37664780-C-T

98823203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, undefined
orthologous variants: 37664815-G-A

98823203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, undefined
orthologous variants: 37664815-G-C

98823203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, undefined
orthologous variants: 37664815-G-T

98823211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous_variant, undefined
orthologous variants: 37664823-G-A

98823211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous_variant, undefined
orthologous variants: 37664823-G-C

98823211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous_variant, undefined
orthologous variants: 37664823-G-T

98823396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense variant
orthologous variants: 37665008-G-T

98823493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: synonymous variant
orthologous variants: 37665105-C-T

98823540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 37665154-G-C

98823540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 37665154-G-T

98823569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37665183-C-G

98823574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37665188-G-T

98823592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37665206-G-T

http://identifiers.org/hco/2/GRCh38#98825928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37666859-C-A

98826922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37667245-G-A

98826922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron variant
orthologous variants: 37667245-G-T

98827098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37667421-T-G

98827160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37667493-C-T

98827186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37667524-A-T

98828023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37667978-G-A

98828077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37668036-T-G

http://identifiers.org/hco/2/GRCh38#98828091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37668051-A-C

98828133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37668074-G-A

98828133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37668074-G-C

98828237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37668165-C-T

98830715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37668995-T-C

98830832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37669107-A-G

98830851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37669126-G-A

98830886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37669173-G-C

98831170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37669436-C-G

98831170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37669436-C-T

98831453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37669712-T-C

98831565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37669824-C-T

98831710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37669939-G-T

98831717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37669946-C-T

98832027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37670187-C-G

98832196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37670271-A-G

http://identifiers.org/hco/2/GRCh38#98832226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37670286-C-A

98832226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37670286-C-T

http://identifiers.org/hco/2/GRCh38#98832227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37670287-C-A

98832227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37670287-C-T

http://identifiers.org/hco/2/GRCh38#98832286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37670339-A-C

98832286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37670339-A-G

http://identifiers.org/hco/2/GRCh38#98832306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37670360-C-A

98832306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37670360-C-T

98832310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37670364-T-A

98832310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37670364-T-G

98832375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37670429-G-A

98832375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37670429-G-C

98832375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37670429-G-T

98832435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37670489-G-A

98832435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37670489-G-C

98832435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37670489-G-T

98832591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37670644-A-G

98832591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37670644-A-T

98832616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37670669-G-A

98832616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37670669-G-T

98832633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37670681-T-C

98832742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37670781-T-C

98833054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37671089-G-A

http://identifiers.org/hco/2/GRCh38#98833096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37671131-C-A

98833096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37671131-C-T

98833215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37671226-G-C

98833274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37671282-G-A

98833638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37671571-C-T

98833720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37671638-G-C

98833896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37671787-A-G

98834021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37671969-A-G

98834021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37671969-A-T

98834307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37672171-A-G

98835073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37672543-G-C

98835077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37672547-A-G

98835176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37672622-A-G

98835180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37672626-A-G

98836468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37675088-C-T

98837940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37675942-A-G

http://identifiers.org/hco/2/GRCh38#98838021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37676811-C-A

98838021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37676811-C-T

98838027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37676817-G-A

98838027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37676817-G-T

98838035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37676825-G-T

98838045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37676834-T-C

98838045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37676834-T-G

98838049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37676838-G-T

98838056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37676845-A-G

98838080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37676887-T-C

98838098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37676922-G-T

98838104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37676928-T-C

98838162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37676985-T-A

98838342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37677158-G-A

98838342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37677158-G-T

98838343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37677159-T-A

98839082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37677901-C-T

98839362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37678161-T-A

98839535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37678331-G-A

98839535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37678331-G-C

98839647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37678490-T-G

98839668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37678521-C-T

98839768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37678618-T-C

98839787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37678637-A-T

98839861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37678708-C-G

98840121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37678898-T-C

98840132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37678911-T-C

98840463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37679224-G-A

http://identifiers.org/hco/2/GRCh38#98845042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37682301-C-A

98845049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37682308-T-C

98845090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37682346-T-C

98845121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37682378-T-C

98845147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37682395-A-T

98845156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37682404-T-C

98845165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37682413-G-C

98845171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37682419-A-T

98845894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37682788-T-A

98845951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37682844-C-T

98846043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37682996-A-G

98846195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683079-T-C

98846195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683079-T-G

98846319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683181-C-G

98846460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683380-T-C

http://identifiers.org/hco/2/GRCh38#98846486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37683406-A-C

98846563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683480-C-T

http://identifiers.org/hco/2/GRCh38#98846618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37683543-C-A

98846625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683550-C-T

98846735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37683646-G-A

98846789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37683700-T-C

98846845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683756-T-C

98846847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683760-G-A

http://identifiers.org/hco/2/GRCh38#98846862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37683775-C-A

98846868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683781-G-A

98846868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683781-G-T

http://identifiers.org/hco/2/GRCh38#98846886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37683799-C-A

98846886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683799-C-G

98846886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683799-C-T

98846899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683813-G-T

http://identifiers.org/hco/2/GRCh38#98846902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37683816-C-A

98846902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683816-C-G

http://identifiers.org/hco/2/GRCh38#98846910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37683824-C-A

98846910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683824-C-G

98846910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683824-C-T

98846913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683827-A-G

98846947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683863-G-A

98846947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683863-G-T

98846951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683867-A-T

98846952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37683868-G-A

http://identifiers.org/hco/2/GRCh38#98846992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37683902-C-A

98847204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37684047-G-A

98847369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37684173-G-A

98847648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37684419-C-T

98847676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37684445-C-T

98848015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37685789-G-C

98848081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37685857-C-T

98848177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37685933-T-C

98848180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37685936-C-T

98848190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37685946-C-T

98848994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37686227-C-T

98849215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37686426-T-C

98849221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37686432-G-A

98849308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37686502-G-A

98849436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37686623-T-A

98849436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37686623-T-C

98849489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37686687-C-G

98849534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37686731-C-T

98849535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37686732-G-A

98849713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37686857-G-T

http://identifiers.org/hco/2/GRCh38#98849748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37686886-A-C

98849854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37686976-T-A

98850128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37689732-G-T

98850176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37689764-C-T

http://identifiers.org/hco/2/GRCh38#98850267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37689837-C-A

98850267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37689837-C-T

98850279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37689852-G-C

98850296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37689869-C-G

98850442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37689988-C-T

98850697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37690214-G-C

98850722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37690240-G-A

98850722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37690240-G-T

98851004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37690501-T-C

98851675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37690812-G-A

98851899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37691002-G-C

98851991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37691041-T-C

98852292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37691272-T-C

98852295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37691275-A-G

98852613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37691605-C-T

98852767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37691740-A-G

98865115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37701311-C-T

98865118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37701314-T-C

http://identifiers.org/hco/2/GRCh38#98865137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37701335-C-A

98865137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37701335-C-T

98865189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37701384-T-C

98865262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37701458-C-G

98865745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37701948-G-A

98866232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37702184-C-T

98866364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37702325-C-G

98867038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37702694-C-T

98867336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37702945-G-C

98867361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37702965-G-A

http://identifiers.org/hco/2/GRCh38#98867455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37703056-C-A

98867455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703056-C-T

98867494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703104-T-C

98867551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703208-T-C

98867600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703258-A-G

98867600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703258-A-T

98867601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703259-C-T

98867602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703260-T-G

98867745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703426-T-C

98867750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703431-G-A

98867833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703518-T-A

98868026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703695-T-C

98868027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703696-C-G

98868037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703706-C-T

98868268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703807-T-C

98868528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37703982-G-C

98868623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37704049-C-T

98868780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37704202-A-G

98868983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37704397-A-G

98869023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37704451-G-T

98869028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37704456-C-T

98869031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37704459-T-C

98869031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37704459-T-G

98869039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37704467-G-A

98869039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37704467-G-T

98869088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37704513-G-A

98869088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37704513-G-T

http://identifiers.org/hco/2/GRCh38#98869268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37704685-A-C

http://identifiers.org/hco/2/GRCh38#98869313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37704730-C-A

98869339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37704756-G-C

98869728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37705638-G-A

98870074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37705933-C-G

http://identifiers.org/hco/2/GRCh38#98870171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#37706030-C-A

98870338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37706192-G-C

98870422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37706277-G-A

98870422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37706277-G-T

98871048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37706314-T-G

98871133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37706369-T-A

98871134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37706370-G-A

98871199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37706417-G-A

http://identifiers.org/hco/2/GRCh38#98871205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37706423-C-A

98871259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37706477-G-T

http://identifiers.org/hco/2/GRCh38#98873585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37707940-C-A

98874522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37709005-G-A

98874690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37709162-C-T

98874881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37709366-T-C

98874892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37709371-T-G

98875012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37709457-C-G

98875017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37709462-C-T

98875086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37709519-C-T

98875196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37709608-T-C

98876211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37710187-T-C

98877018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37710606-C-T

98879409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37713387-G-T

98880807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37714631-G-A

98880894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37714715-T-C

98881175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37715012-G-C

98881226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37715063-C-G

98881226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37715063-C-T

98881241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37715082-G-A

98881549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37715279-G-A

98881596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37715314-G-C

98881659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37715404-A-T

98881741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37715490-A-T

98882348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37716069-G-A

98882388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37716113-T-A

98882439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37716148-G-A

http://identifiers.org/hco/2/GRCh38#98882583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37716251-C-A

98882718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37716398-T-C

98882730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37716410-G-A

98882803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37716485-G-A

98883066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37716734-T-A

98883066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37716734-T-C

98883104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37716771-G-A

98883227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37716884-G-A

98883655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37717259-A-G

98883690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37717293-G-A

98884132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37717695-A-G

98884132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37717695-A-T

98885190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37717941-T-C

98885190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37717941-T-G

98885316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37718070-C-G

98885316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37718070-C-T

98885599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37718337-G-A

98885629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37718364-G-A

98885672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37718404-G-T

http://identifiers.org/hco/2/GRCh38#98885684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37718416-C-A

98885805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37718518-A-G

98885896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37718597-A-G

98886354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37718904-T-C

98892911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37725174-G-T

98893088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37725358-T-A

98893157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37725409-A-G

98893179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37725429-G-C

98893188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37725438-T-C

98896113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37725782-C-G

98896172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37725841-C-T

http://identifiers.org/hco/2/GRCh38#98903426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37728058-A-C

98903529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37728177-C-T

98903568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37728216-C-T

98904091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37728555-G-T

98904222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37728679-C-T

98904366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37728817-G-A

98904366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37728817-G-T

98907823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37731745-C-T

98908089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37732002-G-A

98908089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37732002-G-T

http://identifiers.org/hco/2/GRCh38#98908215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37732076-C-A

98908283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37732153-G-A

98908283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37732153-G-T

98908371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37732450-C-T

http://identifiers.org/hco/2/GRCh38#98908448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37732635-C-A

http://identifiers.org/hco/2/GRCh38#98908469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37732653-C-A

98908501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37732678-G-A

98908501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37732678-G-T

http://identifiers.org/hco/2/GRCh38#98908572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37732745-C-A

98908609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37732780-A-G

98908609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37732780-A-T

http://identifiers.org/hco/2/GRCh38#98908612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37732783-C-A

98908734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37732896-G-A

98909270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37733331-C-T

98909388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37733440-G-T

98909507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37733559-G-A

98909729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37733774-C-G

98910020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37734042-C-G

98911035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37734698-A-T

98911150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37734815-C-T

http://identifiers.org/hco/2/GRCh38#98911285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37734916-C-A

98911340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37734978-G-A

98911530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37735177-G-A

98911530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37735177-G-C

98911760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37735412-G-A

98911957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37735578-G-A

98911961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37735582-G-A

98912215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37735800-T-C

98912272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37735875-A-T

98912276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37735879-G-C

98912283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37735886-G-A

http://identifiers.org/hco/2/GRCh38#98912353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37735939-C-A

98912400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37735986-G-A

http://identifiers.org/hco/2/GRCh38#98912647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37736174-C-A

98912647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37736174-C-T

98912648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37736175-A-G

98912786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37736308-G-A

98912786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37736308-G-C

98912786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37736308-G-T

http://identifiers.org/hco/2/GRCh38#98912832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37736354-C-A

http://identifiers.org/hco/2/GRCh38#98912839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#37736363-C-A

98912875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37736396-A-G

98913315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37736795-G-A

98913396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37736879-G-A

98913523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37737011-T-C

98913587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37737087-G-C

98913587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37737087-G-T

98913743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37737233-C-T

98913960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37737442-G-A

98914046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37737524-A-G

98914120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37737580-T-G

http://identifiers.org/hco/2/GRCh38#98914355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37737925-A-C

98914355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37737925-A-G

98914489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37738103-G-A

98914496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37738107-T-C

98914655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37738267-C-T

98914681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37738278-C-T

98915060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37738626-T-C

98915074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37738636-T-A

98915189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37738702-C-T

98915274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37738763-C-G

98915370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37738862-G-A

98915547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37739025-C-G

98920251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37740790-G-T

98920274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37740813-A-G

98920369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37740914-G-C

98920446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37740969-C-T

98920486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37741006-G-C

98920627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37741201-C-T

98921029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37741510-C-T

98921452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37741806-G-A

98921659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37741991-T-C

98921793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37742134-G-A

98922044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37742396-A-G

98922779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37743264-G-C

98922911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37744107-T-C

98923433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37744378-C-T

98923440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37744383-C-T

http://identifiers.org/hco/2/GRCh38#98923516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37744457-A-C

98923517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37744458-T-C

98923599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37744539-T-C

98923600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37744540-G-A

98923808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37744728-G-A

98924215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37745737-G-A

http://identifiers.org/hco/2/GRCh38#98924398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37745890-A-C

98925620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37747885-T-C

98925623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37747888-G-A

98926119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37748274-C-T

98926322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37748570-C-T

98926573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37748780-G-A

98926702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37748911-T-G

98927005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37749174-G-A

98927038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37749204-C-T

98927140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37749299-T-C

98927140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37749299-T-G

98927149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37749308-T-G

98927388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37749519-T-G

http://identifiers.org/hco/2/GRCh38#98927462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37749594-C-A

98927505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37749627-A-G

98927682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37749771-T-C

98928663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37751311-C-T

98928695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37751343-T-C

98928816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37751474-T-C

98928901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37751569-A-G

98928932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37751598-G-T

98929221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37752586-G-T

98929525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37752835-C-T

http://identifiers.org/hco/2/GRCh38#98929872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37753172-A-C

98930098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37753347-C-T

98930185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37753432-G-T

98930644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37753559-C-T

98931703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37754583-A-G

98931798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37754674-G-A

98932085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37754905-C-T

98932086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37754906-G-A

98932086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37754906-G-T

http://identifiers.org/hco/2/GRCh38#98932110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37754930-A-C

98932124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37754943-C-T

98932180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37754991-C-T

98932429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37755198-C-T

98932520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37755319-T-A

98932520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37755319-T-C

98932911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37755867-C-T

98933255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37756216-C-T

98933659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37756598-T-C

98933711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37756637-C-T

98934218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37757064-A-G

98934218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37757064-A-T

98934254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37757092-A-G

98934343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37757137-G-A

98934588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37757173-G-A

98934700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37757272-C-G

98934773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37757343-T-C

http://identifiers.org/hco/2/GRCh38#98934934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37757535-C-A

98935041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37757631-G-A

98935057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37757648-G-A

98935338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37757983-A-G

98935367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37758021-A-G

98935712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37758386-G-A

http://identifiers.org/hco/2/GRCh38#98935738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37758406-C-A

http://identifiers.org/hco/2/GRCh38#98935844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37758546-C-A

98935844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37758546-C-T

http://identifiers.org/hco/2/GRCh38#98935854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37758564-C-A

98936027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37758733-G-A

98936027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37758733-G-T

98936062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37758779-C-T

98936113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37758828-G-T

98936149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37758864-G-A

98936149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37758864-G-C

98936149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37758864-G-T

98936192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33454
most severe consequence: 5 prime UTR variant
orthologous variants: 37758902-G-A