108167538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130905342-G-A

108167538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130905342-G-C

108167637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 130905243-G-A

108167733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 130905147-C-G

http://identifiers.org/hco/4/GRCh38#108167818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#130905069-C-A

108167818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 130905069-C-T

http://identifiers.org/hco/4/GRCh38#108167993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#130904928-A-C

108168019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904902-G-C

108168019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904902-G-T

108168246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904668-G-A

108168246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904668-G-T

108168301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904599-C-T

108168555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904377-T-C

http://identifiers.org/hco/4/GRCh38#108168573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#130904359-C-A

108168573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904359-C-G

108168626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904306-G-A

108168645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904287-G-A

http://identifiers.org/hco/4/GRCh38#108168662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#130904270-C-A

108168665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904267-A-G

http://identifiers.org/hco/4/GRCh38#108168666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#130904266-C-A

108168777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904129-T-A

108168777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904129-T-C

108168837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904067-G-C

108168837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130904067-G-T

108168920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130903985-C-G

108168920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130903985-C-T

108169035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130903872-G-T

108169087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130903826-T-C

108169092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130903821-T-C

108169095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130903818-T-C

108169146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130903746-G-C

108169502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130903360-A-G

108169620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130903244-G-A

108169724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130903138-T-C

108170671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130902248-G-C

108170671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130902248-G-T

108170678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130902241-A-G

108170843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130902079-A-T

108171108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130901816-A-T

http://identifiers.org/hco/4/GRCh38#108171391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130901576-A-C

108171408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130901560-G-C

108171883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130901100-C-T

108171994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130900965-G-A

108171994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130900965-G-T

http://identifiers.org/hco/4/GRCh38#108172218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130900741-C-A

108172242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900717-G-T

108172245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900714-A-G

108172264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900695-G-A

108172264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900695-G-T

108172303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900653-A-G

108172303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900653-A-T

108172589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900393-G-A

http://identifiers.org/hco/4/GRCh38#108172623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130900359-C-A

108172623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900359-C-T

http://identifiers.org/hco/4/GRCh38#108172674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130900340-C-A

108172674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900340-C-T

108172776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900302-C-G

108172776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900302-C-T

108172788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900288-C-T

108172789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900287-G-A

108172789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130900287-G-T

108172889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130900205-G-T

108172990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 130900121-G-T

108173305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130899819-T-C

108173314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130899810-G-A

108173314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 130899810-G-T

108173418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 130899706-G-A

108173418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 130899706-G-C

108173418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 130899706-G-T

108173995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130899101-A-G

108174086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130899009-C-T

108174091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130899004-A-G

108174231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130898856-G-T

108174278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130898809-G-A

108174373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130898732-C-T

108174414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130898700-G-T

108174888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130898114-G-T

108175035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130897981-G-T

108175284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130897772-C-T

http://identifiers.org/hco/4/GRCh38#108175305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130897756-C-A

108175794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 130897591-G-A

108175833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130897552-A-T

108175943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130897423-A-G

http://identifiers.org/hco/4/GRCh38#108176151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130897215-A-C

108176151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130897215-A-G

http://identifiers.org/hco/4/GRCh38#108176158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130897208-C-A

108176158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130897208-C-T

http://identifiers.org/hco/4/GRCh38#108176215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130897148-C-A

108176215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130897148-C-T

108176252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130897110-G-A

108176291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 130897071-G-A

108176291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 130897071-G-T

108176353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 130897006-A-G

108176643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130896750-A-G

108176643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130896750-A-T

108177060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130896312-T-C

http://identifiers.org/hco/4/GRCh38#108179045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130891894-C-A

108179140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130891802-C-T

108179242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130891694-C-G

108179266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130891672-C-T

108179502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130891477-A-G

108179687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130891417-C-T

108179714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130891390-C-G

108179715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130891389-T-G

108179723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130891383-G-A

108179758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130891328-C-G

108182598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130889973-T-A

108182598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130889973-T-C

108182720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130889851-A-G

108182746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130889814-C-G

108182746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130889814-C-T

108182752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130889808-A-G

108182784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130889777-A-G

108182921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130889663-A-G

108182997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130889592-C-T

108183045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130889545-T-C

http://identifiers.org/hco/4/GRCh38#108183073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130889517-C-A

108183073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130889517-C-G

108183636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130888757-A-T

http://identifiers.org/hco/4/GRCh38#108183865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130888462-C-A

108183939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130888396-T-C

108184053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130888281-A-G

108184194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130888126-T-C

108184701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130887644-C-T

108185214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130886499-G-A

108185583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130886154-A-G

108185615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130886068-A-G

http://identifiers.org/hco/4/GRCh38#108185759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130885932-A-C

108187782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130885708-G-T

108187800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130885690-T-A

108187898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130885628-T-C

108187930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130885610-G-A

108188193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130885345-C-T

108188373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130885183-T-C

108188403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130885170-T-C

108188757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130883530-G-T

108188956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130883329-G-A

108192695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130880582-C-G

108192709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130880570-A-G

108192734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130880540-T-G

108192770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130880505-G-T

108193130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130879850-G-C

108193892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130879083-A-G

108193910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130879067-C-T

108194099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130878880-A-G

108194203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130878798-A-T

108194385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130878601-G-A

108195059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130877740-G-A

108195059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130877740-G-C

108195255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130877434-A-G

108195317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130877365-C-T

108197835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130876111-T-C

108197897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130876051-G-A

108197958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130875996-G-A

http://identifiers.org/hco/4/GRCh38#108197994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130875938-C-A

108197994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130875938-C-G

108197994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130875938-C-T

108198347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130875247-A-G

108199337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130873467-A-G

http://identifiers.org/hco/4/GRCh38#108199365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130873439-C-A

108199431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130873373-G-A

108199472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130873335-C-G

108199564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130873243-G-A

108199564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130873243-G-C

108199746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130873015-C-G

108199811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130872945-T-C

108199811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130872945-T-G

108200429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130872316-G-A

108201817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130871306-A-G

108201860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130871262-T-C

108202064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130871095-T-C

108202078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130871081-A-T

108202378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130870190-T-A

http://identifiers.org/hco/4/GRCh38#108202450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130870117-A-C

108210861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130867198-G-A

108211147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130866919-T-A

108211403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130866693-A-G

108211403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130866693-A-T

108211515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130866591-G-A

108211692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130866413-G-A

108212358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130865395-A-T

108212994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130864449-A-G

108213869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130863530-T-C

108214096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130863324-G-A

108214167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130863232-C-T

108214259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130863161-T-C

108214268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130863152-C-T

108214489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130862959-A-G

108215033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130862467-A-G

108215247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130862235-G-C

108215276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130862207-C-G

108215330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130862148-C-T

108215657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130861842-G-A

108215684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130861815-T-C

108215856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130861612-G-A

108216027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130861434-G-C

108218475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130860686-G-A

108219186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130859935-G-A

108219276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130859842-A-G

108219285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130859833-G-A

108219285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130859833-G-C

108221499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130857001-A-G

108221607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130856580-C-G

108221609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130856578-G-A

108221670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130856518-C-T

http://identifiers.org/hco/4/GRCh38#108221700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130856488-A-C

108221755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130856434-T-A

108221846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130856338-A-G

108222252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130855479-T-A

108222405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130855324-G-A

108222569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130855165-G-T

108223209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130854620-G-A

108223209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130854620-G-C

108223417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130854425-G-A

108224863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130854020-G-A

108225031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130853833-T-C

108225377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130853489-G-A

108225378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130853488-T-A

108225486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130853401-G-A

108225577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130853310-G-A

108225631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130853266-G-A

108225660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130853240-C-T

108225908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130852301-C-G

108225908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130852301-C-T

108228800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130850183-T-C

http://identifiers.org/hco/4/GRCh38#108229106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130849863-A-C

108229208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130849704-C-G

108229208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130849704-C-T

108235710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130849085-C-T

108236106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130848706-A-T

108236123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130848681-T-G

108236168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130848653-G-A

108236168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130848653-G-C

108236168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130848653-G-T

108236172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130848649-G-A

108236173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130848648-G-A

108236189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130848627-G-C

108236247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130848544-C-G

108236247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130848544-C-T

108236927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130847931-T-C

108237105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130847770-T-A

108237121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130847754-C-T

108237434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130846577-G-C

108237679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130846369-G-A

http://identifiers.org/hco/4/GRCh38#108238230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130845846-C-A

108238230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130845846-C-T

108238348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130845726-C-T

108239109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130845615-G-A

108239340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130845384-A-G

108239736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130845002-C-G

108240990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130844062-A-T

108241314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130843234-A-G

108241700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130842733-A-G

108241872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130842575-T-C

108242244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130841843-T-A

108242262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130841825-A-G

http://identifiers.org/hco/4/GRCh38#108242301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130841786-C-A

108242536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130841560-G-A

108242536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130841560-G-T

108242608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130841493-C-T

108242821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130841044-A-G

108243466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130840278-G-A

108243604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130840159-T-C

108244043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130839688-C-G

108245209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130839440-T-A

108245384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130839267-A-G

108245461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130839217-G-T

108245647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130839056-G-A

108246119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130838639-G-A

http://identifiers.org/hco/4/GRCh38#108246237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130838525-C-A

108246237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130838525-C-T

108246262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130838500-A-G

108246389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130838395-C-T

108246449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130838330-T-C

108246751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130838006-A-G

108246892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130837874-A-T

108246895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130837871-T-C

108247050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130837742-A-G

108247073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130837726-G-A

108248345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130836989-C-G

108250026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130833811-G-A

108250139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130833696-T-C

108250253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130833492-A-T

http://identifiers.org/hco/4/GRCh38#108250266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130833467-A-C

108250624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130833053-T-G

108251401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130833002-G-T

108251428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130832971-A-G

108251580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130832847-A-G

108251668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130832774-A-G

108251749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130832693-T-C

108251796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130832645-T-C

108251796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130832645-T-G

http://identifiers.org/hco/4/GRCh38#108251978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130832429-C-A

108252873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130832089-G-A

108253093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130831288-A-T

108253094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130831287-A-G

108253777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130828980-A-G

108253863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130828894-C-T

http://identifiers.org/hco/4/GRCh38#108254035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130828775-A-C

108254428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130828425-A-G

108254566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130828251-A-G

108254566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130828251-A-T

108254586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130828230-C-T

108254669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130828155-A-G

108254921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130827935-G-A

108254921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130827935-G-T

108254995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130827881-C-T

108255161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130827407-G-T

108255180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130827405-G-A

108255238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130827347-G-C

108255238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130827347-G-T

108255287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130827300-G-A

108255416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130826801-C-T

http://identifiers.org/hco/4/GRCh38#108255466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#130826758-C-A

108255641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130826589-G-A

108255737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130826506-T-C

108256173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130826091-A-G

108256499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130825791-G-A

108256526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130825771-T-G

108256574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130825723-C-T

108256579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 130825718-A-T

108256926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: non coding transcript exon variant
orthologous variants: 130825373-A-G

108257649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: non coding transcript exon variant
orthologous variants: 130824757-T-G

108257739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: non coding transcript exon variant
orthologous variants: 130824674-C-G

108257839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: non coding transcript exon variant
orthologous variants: 130824571-G-A

108257839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40339
most severe consequence: non coding transcript exon variant
orthologous variants: 130824571-G-T