43194596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 3 prime UTR variant
orthologous variants: 118068444-G-C

43194596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 3 prime UTR variant
orthologous variants: 118068444-G-T

43194826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 3 prime UTR variant
orthologous variants: 118068198-G-T

http://identifiers.org/hco/10/GRCh38#43194926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118068102-C-A

43194926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 3 prime UTR variant
orthologous variants: 118068102-C-T

43195499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 3 prime UTR variant
orthologous variants: 118067601-G-T

43195520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 3 prime UTR variant
orthologous variants: 118067546-T-G

43195914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 3 prime UTR variant
orthologous variants: 118067140-A-T

43196227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 3 prime UTR variant
orthologous variants: 118066813-C-T

43196275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 118066768-G-A

43196275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 118066768-G-C

43196407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118066609-G-T

43196409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118066607-A-G

http://identifiers.org/hco/10/GRCh38#43196423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118066590-C-A

43197181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065998-G-T

43197225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065948-A-G

43197225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065948-A-T

43197227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065946-T-A

43197227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065946-T-C

43197228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065945-G-T

43197312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065868-G-T

http://identifiers.org/hco/10/GRCh38#43197507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118065706-C-A

43197546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065658-C-T

43197659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065604-G-A

43197704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065558-T-A

43197704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065558-T-C

43197744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065515-C-T

43197758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065501-T-C

43197902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065368-G-A

43197902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065368-G-T

http://identifiers.org/hco/10/GRCh38#43197928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118065345-C-A

43198128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: missense variant
orthologous variants: 118065135-G-A

43198289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065007-G-A

43198289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118065007-G-T

http://identifiers.org/hco/10/GRCh38#43198326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118064970-C-A

43198326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118064970-C-T

43198784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118064354-G-A

43198784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118064354-G-C

43198784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118064354-G-T

43198799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118064339-G-A

43198799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118064339-G-T

http://identifiers.org/hco/10/GRCh38#43198853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118064302-C-A

43198853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118064302-C-T

http://identifiers.org/hco/10/GRCh38#43198854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118064301-C-A

43198854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118064301-C-T

http://identifiers.org/hco/10/GRCh38#43199226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118063954-C-A

43199265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063930-G-A

43199265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063930-G-T

http://identifiers.org/hco/10/GRCh38#43199446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118063490-C-A

43199500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063437-G-A

43199526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063407-G-A

43199526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063407-G-T

43199544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063382-G-A

43199544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063382-G-C

43199544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063382-G-T

43199580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063354-T-C

43199609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063336-G-T

43199643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063301-A-G

43199728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: missense variant
orthologous variants: 118063216-T-C

43199762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: missense variant
orthologous variants: 118063182-C-G

43199796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063149-G-T

43199797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063148-G-A

43199797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063148-G-C

43199797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063148-G-T

43199805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063140-G-T

43199809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063136-A-G

http://identifiers.org/hco/10/GRCh38#43199900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118063060-C-A

43199900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118063060-C-T

43200040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118062954-G-T

43200041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118062953-T-A

43200041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118062953-T-G

http://identifiers.org/hco/10/GRCh38#43200072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118062922-C-A

43200072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118062922-C-T

43200078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118062916-A-G

43200078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118062916-A-T

43200125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118062869-G-C

43200180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: splice donor variant
orthologous variants: 118062808-A-G

43200204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118062784-A-G

43200289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118062716-A-G

43200324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118062690-A-T

http://identifiers.org/hco/10/GRCh38#43200331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118062683-C-A

43200331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118062683-C-T

43200332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118062682-A-G

43200332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118062682-A-T

43200479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118062644-A-G

43200575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118062546-G-T

43200619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118062492-G-T

http://identifiers.org/hco/10/GRCh38#43200965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118062142-C-A

http://identifiers.org/hco/10/GRCh38#43201039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118062072-C-A

43201039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118062072-C-T

43201340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118061838-C-T

http://identifiers.org/hco/10/GRCh38#43201678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118061630-C-A

43201678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118061630-C-T

43201716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118061604-A-G

43201716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118061604-A-T

43201739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118061577-C-G

http://identifiers.org/hco/10/GRCh38#43201749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118061567-C-A

43201800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118061525-G-A

43201923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118061402-G-A

43201923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118061402-G-C

http://identifiers.org/hco/10/GRCh38#43201955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118061369-C-A

43201970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118061358-A-G

43201999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118061329-G-T

43202007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118061321-A-G

43202015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118061313-A-G

http://identifiers.org/hco/10/GRCh38#43202030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118061291-C-A

43202030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118061291-C-T

43202193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118061140-C-G

43202193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118061140-C-T

43202364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118060980-G-C

43202424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118060941-A-G

43202424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118060941-A-T

43202470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118060898-C-T

http://identifiers.org/hco/10/GRCh38#43202578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#118060817-C-A

http://identifiers.org/hco/10/GRCh38#43202615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#118060781-C-A

43202615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118060781-C-T

43202641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060770-G-A

43202641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060770-G-C

43202641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060770-G-T

http://identifiers.org/hco/10/GRCh38#43202691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#118060710-C-A

http://identifiers.org/hco/10/GRCh38#43202766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118060651-C-A

43202766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060651-C-G

43202766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060651-C-T

http://identifiers.org/hco/10/GRCh38#43202861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118060532-A-C

43203004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060377-G-A

43203004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060377-G-C

43203004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060377-G-T

43203010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060371-T-A

43203010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060371-T-C

http://identifiers.org/hco/10/GRCh38#43203035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118060350-C-A

http://identifiers.org/hco/10/GRCh38#43203040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118060345-C-A

43203040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060345-C-G

43203048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060336-G-A

http://identifiers.org/hco/10/GRCh38#43203086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118060302-A-C

43203086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060302-A-G

43203113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060260-T-A

43203113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060260-T-G

http://identifiers.org/hco/10/GRCh38#43203115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118060258-A-C

43203115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060258-A-G

43203127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060241-G-A

43203127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060241-G-C

43203127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060241-G-T

http://identifiers.org/hco/10/GRCh38#43203171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118060198-C-A

43203179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060191-T-A

43203179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060191-T-C

43203205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060161-A-G

http://identifiers.org/hco/10/GRCh38#43203206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118060160-C-A

43203206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060160-C-G

43203206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060160-C-T

http://identifiers.org/hco/10/GRCh38#43203207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118060159-C-A

43203207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060159-C-T

43203254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060124-C-T

43203255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060123-T-A

43203255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060123-T-G

43203280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118060105-A-G

http://identifiers.org/hco/10/GRCh38#43203428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118059965-C-A

43203428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118059965-C-G

43203428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118059965-C-T

43203432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118059961-A-G

http://identifiers.org/hco/10/GRCh38#43203446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118059953-C-A

43203446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118059953-C-G

43203446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118059953-C-T

43203474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118059925-G-A

43203474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118059925-G-C

43203474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118059925-G-T

http://identifiers.org/hco/10/GRCh38#43203480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118059924-C-A

43203480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118059924-C-T

43203484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118059920-G-A

43203484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118059920-G-T

http://identifiers.org/hco/10/GRCh38#43203543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118059889-C-A

43203543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118059889-C-G

43203543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118059889-C-T

http://identifiers.org/hco/10/GRCh38#43203571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118059867-C-A

43203571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118059867-C-T

43204084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118059750-G-A

43204323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118059500-G-A

43204338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118059485-A-G

43204372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118059443-C-T

43204461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118059364-G-A

43204502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118059350-G-A

43204507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118059345-A-G

43204783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118059081-G-T

43205115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118058234-G-A

43205175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118058168-G-C

43205182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118058159-A-T

43205222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118058132-C-T

43205365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, undefined
orthologous variants: 118057978-G-C

43205368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, undefined
orthologous variants: 118057975-G-A

43205425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057919-G-A

http://identifiers.org/hco/10/GRCh38#43205447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118057904-C-A

43205448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057903-A-G

43205557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057822-C-T

43205631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057790-C-T

43205656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057763-G-A

43205757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057679-G-A

http://identifiers.org/hco/10/GRCh38#43205789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118057646-C-A

http://identifiers.org/hco/10/GRCh38#43205802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118057633-C-A

43205802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057633-C-T

http://identifiers.org/hco/10/GRCh38#43205814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118057622-C-A

43205814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057622-C-G

43205814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057622-C-T

43205838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057598-G-A

43205838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057598-G-T

http://identifiers.org/hco/10/GRCh38#43205853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118057583-C-A

43205859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057577-A-G

43205859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057577-A-T

43205885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057554-A-T

43205892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057547-T-C

43205971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: missense variant
orthologous variants: 118057468-G-T

http://identifiers.org/hco/10/GRCh38#43206251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118057243-C-A

43206251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057243-C-T

43206300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118057206-C-T

43206545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056928-T-A

43206545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056928-T-C

43206562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056912-A-G

http://identifiers.org/hco/10/GRCh38#43206573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118056905-C-A

43206573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056905-C-T

43206578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056900-G-A

43206578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056900-G-C

43206578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056900-G-T

43206625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056818-G-A

43206634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056809-G-C

43206634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056809-G-T

43206635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056808-C-T

43206681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056742-T-C

43206681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118056742-T-G

43206755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118056659-G-A

43206761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118056650-A-G

43206783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118056628-A-G

43206828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118056590-G-A

43206828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118056590-G-T

43206853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118056564-T-C

43206853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118056564-T-G

43206885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118056541-G-A

http://identifiers.org/hco/10/GRCh38#43206936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118056500-C-A

43206936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118056500-C-T

43206956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118056481-A-T

43210678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118055378-T-C

43210739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118055322-A-G

43210786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118055274-A-G

43211041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118055160-C-G

43211046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118055155-T-C

43211377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118054818-C-G

43211391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118054804-C-T

43211480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118054712-C-G

43211513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118054675-C-T

43211550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118054638-G-A

43211573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118054605-C-T

43211832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118054303-G-A

43211844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118054291-G-C

43211901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118054238-G-T

43212096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118054045-C-T

43212315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118053816-G-A

43212416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118053759-C-T

43212423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118053752-C-T

43212448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118053727-C-T

43214584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118052086-G-C

43214763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118051928-A-T

43214857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118051832-C-T

43215302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118051392-G-C

43215401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118051294-A-G

43215402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118051293-T-C

43215547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118051152-C-T

43215571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118051111-T-C

43215641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118051041-A-G

43218428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118049201-G-T

43218615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118048795-A-G

43218705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118048671-A-G

43218805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118048565-G-T

43218908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118048460-G-C

43218909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118048459-A-G

43218942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118048426-C-T

43218996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118048361-G-C

43219235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118048126-G-A

43219269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118048087-C-T

43219371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118048006-C-T

43219430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118047965-C-G

43219653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118047802-G-A

43219657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118047798-G-A

43219657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118047798-G-T

43219740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118047723-C-G

43220067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118047382-G-A

43227661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118045484-G-A

43228429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118044885-G-A

43228525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118044796-C-T

43228583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118044728-T-C

43228652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118044674-A-G

43228735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118044570-A-G

43228830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118044294-C-G

43228978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118044155-C-T

43229185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118044011-C-T

43229565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118043493-G-A

43229565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118043493-G-T

43229777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118043304-T-C

43229831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118043286-G-C

43229831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118043286-G-T

http://identifiers.org/hco/10/GRCh38#43229836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118043281-C-A

43229836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118043281-C-T

43230068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118043105-G-A

43230068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118043105-G-C

43230165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118043031-G-A

43230165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118043031-G-T

43230295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118042904-G-A

43230347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 118042858-G-A

http://identifiers.org/hco/10/GRCh38#43230539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118042671-C-A

43230547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118042663-C-T

http://identifiers.org/hco/10/GRCh38#43230799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118042431-C-A

43230799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118042431-C-G

43230955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118042288-G-T

43231050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118042210-C-G

43231050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118042210-C-T

43231896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118041613-G-A

43232039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118041486-G-A

http://identifiers.org/hco/10/GRCh38#43233069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118041161-A-C

43233733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118040364-C-T

43233801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118040292-A-G

43249456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118030551-C-T

43251126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118028467-G-A

43251954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118027187-T-G

43251956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118027183-C-T

43254455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, undefined
orthologous variants: 118025663-G-A

43254525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, undefined
orthologous variants: 118025599-C-T

43254705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, undefined
orthologous variants: 118025444-C-T

43254785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118025375-G-T

43254840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118025323-C-T

43255220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118024911-C-T

43255542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118024601-G-A

43255693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, undefined
orthologous variants: 118024467-A-G

43255749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 118024431-G-A

43255800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron_variant, undefined
orthologous variants: 118024394-G-A

43258001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117993852-A-G

43258493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117993435-G-A

43258498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117993430-A-T

http://identifiers.org/hco/10/GRCh38#43262203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117993199-C-A

43262203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117993199-C-T

43262387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117993007-C-T

43262512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117992893-G-A

43262640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117992748-G-T

43262784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117992609-C-T

43263098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117992332-G-A

43263265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117992134-A-G

43263420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117991980-G-A

43263623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117991629-G-A

43263660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117991592-A-G

http://identifiers.org/hco/10/GRCh38#43264313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117990933-C-A

43264372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117990892-G-A

43264779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117990534-G-A

43264779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117990534-G-C

43264794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117990519-G-A

43264794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117990519-G-C

43265009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117990317-C-T

43265024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117990302-T-C

43265197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117990163-G-A

43265197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117990163-G-C

43265365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117989958-A-G

43265565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117989664-C-T

43265749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117989531-C-T

43265909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117989383-G-A

43265950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117989342-A-G

43266376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117988893-G-T

http://identifiers.org/hco/10/GRCh38#43266483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117988788-C-A

43266582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117988701-G-A

43266646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117988642-G-A

43266768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117988589-G-A

43266768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: intron variant
orthologous variants: 117988589-G-T

43266850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5 prime UTR variant
orthologous variants: 117988517-T-A

http://identifiers.org/hco/10/GRCh38#43267049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24246
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117988320-A-C