37120426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 44756497-C-T

http://identifiers.org/hco/9/GRCh38#37120539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44756608-C-A

37120870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44756922-G-C

37120870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44756922-G-T

37121162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44757214-C-T

37121240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44757275-C-G

37121301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44757325-A-G

37122310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44758462-C-G

37123088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44758973-G-A

37123208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44759085-T-A

37123208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44759085-T-C

37123217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44759094-G-A

37123530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44759396-C-T

37123979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44759994-G-A

37124535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44760517-C-G

37126304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44761842-T-C

37126304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44761842-T-G

37127382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44762876-G-A

37127425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44762914-T-A

37128172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44763890-G-A

37128261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44763954-T-C

37134557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44768111-C-G

37135238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44768634-A-G

37135933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44769200-A-G

37135938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44769205-G-C

37136460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44769510-G-T

37136909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44769891-G-A

37138744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44772862-G-A

37138744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44772862-G-T

37139363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44773424-C-T

http://identifiers.org/hco/9/GRCh38#37139749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44773727-C-A

37139749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44773727-C-G

37139854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44773844-T-G

37139877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44773867-A-G

37139914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44773902-A-G

37140707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44774645-T-C

http://identifiers.org/hco/9/GRCh38#37140816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44774744-C-A

37140959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44774880-A-G

37141036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44774950-A-G

37141124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44775032-A-G

37141346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44775269-A-G

37141752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44775667-C-T

37142013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44775948-A-G

37142697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44776514-A-T

37143864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44777548-A-G

37144078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44777761-T-C

37144125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44777813-G-A

37144149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44777836-G-A

http://identifiers.org/hco/9/GRCh38#37144854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#44778458-C-A

37144854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44778458-C-G

37145132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44778736-T-C

37145766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44779310-G-A

37145968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44779535-C-T

37146167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44779776-G-A

37146195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44779805-G-A

37146285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44779887-T-C

37146557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44780064-G-A

37146557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44780064-G-C

37146642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44780154-A-G

37146659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44780171-G-A

37147199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44781024-C-T

37147213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44781038-T-C

37147546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44781366-A-G

37147896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44781849-G-A

37148011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44781927-T-A

37148367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44782237-T-C

37148402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44782267-G-A

37149264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44782876-T-C

37150084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44783687-A-T

37150192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44783794-T-G

37150360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44783943-C-T

37150439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44784024-C-G

37150439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44784024-C-T

37151896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44784908-C-G

37155922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44786241-G-A

37156250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44787159-G-C

37157600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44790077-C-T

37157646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44790122-G-A

37157672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44790148-C-T

37157826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44790297-G-C

37158170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44790588-T-C

37158183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44790601-G-T

http://identifiers.org/hco/9/GRCh38#37158393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44790802-A-C

37158393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44790802-A-G

37158743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44791084-C-T

37158836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44791176-A-G

http://identifiers.org/hco/9/GRCh38#37159322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44791644-C-A

37159462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44791731-A-G

37161829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44792516-C-T

37173737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44794530-A-G

37174640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44797114-A-G

37174816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44797332-G-A

37177725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44797962-G-A

37180922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44801498-T-A

37180922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44801498-T-C

37180940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44801517-A-T

37183150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44803343-T-C

37183558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44803959-G-A

37186747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44805526-A-G

37186810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44805612-G-A

37186810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44805612-G-T

37186821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44805628-A-G

37186828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44805635-T-C

37186853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44805714-C-T

37186921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44805775-T-C

http://identifiers.org/hco/9/GRCh38#37186953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44805817-C-A

http://identifiers.org/hco/9/GRCh38#37186967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44805831-C-A

37191811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44807662-T-C

37192212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44808052-C-T

37192403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44808238-C-T

37192738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44808569-A-G

37192862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44808694-A-G

37193063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44808895-A-G

37193480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44809247-A-G

37195562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44812393-A-T

37195584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44812411-A-G

37196284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44813064-T-G

37196849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44813587-G-A

37197035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44813725-G-A

37197059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44813749-A-G

37197526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44814204-T-G

37197595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44814263-T-C

37197624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44814297-T-C

37198026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44814639-G-A

37198805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44815406-C-G

37198935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44815533-T-A

37198985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44815583-T-C

37198993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44815591-T-A

37199144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44815729-A-G

37199145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44815730-T-C

37199203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44815768-C-T

http://identifiers.org/hco/9/GRCh38#37199218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44815782-C-A

37199218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44815782-C-T

37199274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44815834-G-T

37200296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44816109-C-T

37200405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44816176-T-C

37201997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44816979-G-C

37203059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44817636-G-T

37207930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44822568-A-G

37209719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44823645-T-A

37209953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44823861-A-G

37210175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44824093-G-A

37210259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44824177-A-G

37210282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44824200-A-G

37210728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44824794-A-G

37211094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44825125-A-G

http://identifiers.org/hco/9/GRCh38#37211500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#44825489-A-C

http://identifiers.org/hco/9/GRCh38#37212092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44825890-A-C

37212092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44825890-A-G

37212092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44825890-A-T

37212320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44826108-A-T

37212359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44826137-A-G

37212618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44826431-A-G

37212730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44826664-C-T

37212747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44826681-C-T

37212940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44826897-C-T

http://identifiers.org/hco/9/GRCh38#37213061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44827103-A-C

37213061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44827103-A-T

37213277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44828637-T-C

37213278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44828638-G-A

37213750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44829050-T-C

37213827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44829127-A-G

37214919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44830183-T-C

37215139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44830384-C-T

http://identifiers.org/hco/9/GRCh38#37216149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44831350-A-C

37216149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44831350-A-G

37231797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44834620-G-T

37233150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44836325-A-G

37236361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44838286-G-A

37236723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44838351-T-G

37236998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44838625-A-G

37237524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44839126-A-G

37237733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44839379-G-A

37238375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44840105-C-T

37238974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44840717-A-G

37239042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44840783-G-T

37239312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44841025-G-C

37239905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44841597-A-T

37240019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44841750-G-A

37240046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44841783-T-G

37240819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44842307-G-C

37241799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44843235-T-G

37241860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44843285-C-G

37242217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44843686-G-A

37242415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44843882-A-G

37242428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44843894-C-T

http://identifiers.org/hco/9/GRCh38#37243575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44845013-C-A

37243742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44845166-C-G

37243883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44845296-C-T

37243884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44845297-A-G

37244061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44845464-A-T

http://identifiers.org/hco/9/GRCh38#37244184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44845586-A-C

37244853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44846207-C-T

37245564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44846697-C-T

37245838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44846869-A-G

37246083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44847111-G-A

37246083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44847111-G-C

37246159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44847164-G-T

37246171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44847176-A-G

37246194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44847199-G-A

37246528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44847467-G-A

37247907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44848526-A-T

37247946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44848575-G-A

37248149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44848751-G-T

37250743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44851191-A-T

37252536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44852884-T-C

37253507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44853907-C-T

37253858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44854243-A-G

37254047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44854607-A-G

37254281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44854824-T-C

37255958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44857822-C-T

37256023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44857880-G-C

37256225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44858709-T-C

37256231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44858715-G-A

37259468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44859858-T-A

37259468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44859858-T-C

37260006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44860435-A-G

37260224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44860611-T-A

37260224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44860611-T-C

37260225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44860612-G-C

37260387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44860762-A-G

37260444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44860815-C-T

37261224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44861422-G-A

37261459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44861640-C-T

37261736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44862130-G-A

37261814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44862195-G-T

37262100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44862501-G-A

37262238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44862665-G-T

37262347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44862786-G-A

37262464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44862892-T-C

37262536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44862952-C-T

37262616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44863028-A-G

37263010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44863351-T-A

http://identifiers.org/hco/9/GRCh38#37264002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44864648-C-A

37264002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44864648-C-T

37264057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44864694-C-T

http://identifiers.org/hco/9/GRCh38#37264300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44864938-C-A

37264300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44864938-C-T

http://identifiers.org/hco/9/GRCh38#37264503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44865095-C-A

http://identifiers.org/hco/9/GRCh38#37264580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44865162-A-C

37264689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44865313-T-C

37264689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44865313-T-G

37264729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44865434-A-G

37264793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44865569-C-T

37264946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44865678-A-G

37265651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44866092-C-T

37268278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44866562-C-T

37270807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44872239-T-A

37270986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44872417-A-G

http://identifiers.org/hco/9/GRCh38#37271437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44872877-A-C

37271437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44872877-A-T

37271552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44872952-A-G

37272102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44873191-T-C

37272281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44873512-A-G

37272711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44873884-G-C

37272788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44873965-C-G

37276017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44876092-A-G

37276034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44876109-G-A

37276571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44876799-A-G

37276784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44877011-G-A

37276972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44877167-C-G

37276999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44877196-G-A

37277012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44877210-C-T

37277084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44877288-A-G

37277858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44877892-A-G

37278209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44878004-G-A

37278271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44878053-A-G

37278271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44878053-A-T

37283063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44879428-T-C

37283266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44879651-C-T

37283820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44880192-C-T

37284577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44880917-C-T

37285322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44881595-G-A

37285527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44881756-T-C

37285583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44881816-G-A

37285879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44882224-A-G

37285879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44882224-A-T

37287328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44882574-A-G

37287328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44882574-A-T

37287376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44882594-A-T

37287915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44880917-C-T

37288447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44882965-T-C

37288483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44883002-G-T

37289081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44883498-G-A

37289368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44883564-C-G

37289773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44883851-T-G

http://identifiers.org/hco/9/GRCh38#37290182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44884196-A-C

37292749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44884338-A-G

37292917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44884492-G-A

37293000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44884575-A-G

37293055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44884623-A-T

37293534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44885328-T-A

37293534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44885328-T-C

37294411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44886436-T-G

37294628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44886820-A-G

37294768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44886935-T-C

37295009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44887378-T-C

37295109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44887478-A-G

37300991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44891733-T-G

37301002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44891748-T-G

37302053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44893392-G-A

37302145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44893495-T-C

37302154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44893504-G-A

37302154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44893504-G-T

37302241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44893580-A-G

http://identifiers.org/hco/9/GRCh38#37302257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#44893587-C-A

37302257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44893587-C-G

37302257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44893587-C-T

37302417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44893775-G-A

37303105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44894578-A-G

37303125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44894598-T-C

http://identifiers.org/hco/9/GRCh38#37304033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44894769-A-C

37304099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44894835-T-C

37304116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44894844-A-G

37304138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44894866-T-C

http://identifiers.org/hco/9/GRCh38#37304181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44894909-C-A

37304181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44894909-C-G

37304181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44894909-C-T

37304396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44895112-G-A

37304396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44895112-G-C

http://identifiers.org/hco/9/GRCh38#37304398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44895114-A-C

37304398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44895114-A-G

37304428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44895138-T-A

37304428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44895138-T-C

37305232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44895520-T-C

37305418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44895693-T-A

37305437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44895712-G-T

37305472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44895735-T-C

37307242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44896652-A-G

http://identifiers.org/hco/9/GRCh38#37307245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44896655-C-A

37307302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44896698-C-T

37310020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44897029-T-C

37314455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44900655-A-T

37315116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44901090-G-C

37315116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44901090-G-T

37315168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44901141-G-A

37315168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44901141-G-T

37320959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44902760-G-A

37320959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44902760-G-T

37322396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44903694-G-A

37322396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44903694-G-T

37322621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44903894-G-A

37322727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44904002-T-C

37322747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44904020-T-G

37323088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44904305-A-G

37323278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44904659-A-G

37323874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44905251-C-T

37323942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44905314-G-A

37323945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44905317-T-G

37323961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44905334-C-G

37324007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44905377-T-C

37324362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44905733-G-A

37325213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44906584-A-G

http://identifiers.org/hco/9/GRCh38#37325675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44906972-C-A

37325675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44906972-C-T

37325679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44906976-G-A

37326035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44907201-G-A

37326411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44907508-T-C

37326943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44907707-A-T

37327012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44907768-G-A

37327012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44907768-G-C

37327149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44907853-T-G

37327166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44907870-A-G

http://identifiers.org/hco/9/GRCh38#37327325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44908048-C-A

37327418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44908090-A-G

37327418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44908090-A-T

37327503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44908166-G-A

37328588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44909217-C-T

37328996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44909507-T-C

37329128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44909650-T-C

37329543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44909997-T-C

37329632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44910089-A-G

37330980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44911420-A-G

37331434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44911850-G-A

37331441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44911857-T-C

37331467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44911885-A-G

37331566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44911976-T-C

37331987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44912450-A-T

37332368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44912881-G-T

37332408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44912909-C-T

37332660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44913123-C-G

37333301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44913670-A-T

37333349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44913704-A-T

37333499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44913841-C-T

37333504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44913846-C-T

37333511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44913853-G-A

37333519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44913861-T-G

37334543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44914673-G-C

37334703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44914829-T-C

37334786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44914884-A-G

37335411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44915801-A-G

37335496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44915885-G-C

37335771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44916097-A-G

37336340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44916911-C-G

http://identifiers.org/hco/9/GRCh38#37336376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44916947-A-C

37336376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44916947-A-G

37336376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44916947-A-T

37336439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44917065-T-C

http://identifiers.org/hco/9/GRCh38#37336613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44917347-A-C

37336613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44917347-A-T

37336618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44917352-T-C

37336713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44917403-T-A

37336713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44917403-T-C

http://identifiers.org/hco/9/GRCh38#37336918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44917609-A-C

37336918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44917609-A-G

37336918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44917609-A-T

http://identifiers.org/hco/9/GRCh38#37337360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44918045-C-A

http://identifiers.org/hco/9/GRCh38#37337414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44918085-C-A

37337414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44918085-C-G

37337414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44918085-C-T

http://identifiers.org/hco/9/GRCh38#37337415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44918086-C-A

37337415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44918086-C-G

http://identifiers.org/hco/9/GRCh38#37337416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44918087-A-C

http://identifiers.org/hco/9/GRCh38#37337417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44918088-A-C

37337417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44918088-A-G

37338095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44918763-A-T

37338460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44919118-T-A

37338460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44919118-T-C

37338885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44919542-C-T

37339145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44919777-G-A

37340878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44922054-G-A

37341086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44922282-C-T

37341449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44922640-G-T

37344475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44923490-T-C

37344587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44923604-A-G

37345889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44924630-G-A

37345889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44924630-G-C

37349592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44926211-T-C

37350631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44926568-G-A

37350631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44926568-G-C

37350631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44926568-G-T

37350694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44926613-G-T

37351140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44927016-G-A

37351241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44927117-G-A

37351621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44927299-T-A

37352244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44927893-A-G

37354216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44928653-A-T

37354436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44928884-A-G

37354547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44928957-T-G

37354738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44929149-C-T

37354928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44929338-G-A

37355270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44929790-A-G

37355921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44930326-T-G

37356140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44930433-G-A

37356174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44930460-T-C

37356261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44930526-T-C

37356381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44930649-A-G

37356583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44930810-T-A

37356583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44930810-T-C

37356854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44931055-T-C

http://identifiers.org/hco/9/GRCh38#37357012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44931210-A-C

37357125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44931320-C-T

37357182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44931377-G-C

37357207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44931401-G-A

http://identifiers.org/hco/9/GRCh38#37357394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44931552-C-A

37357410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44931568-T-A

37357410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44931568-T-C

http://identifiers.org/hco/9/GRCh38#37357726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44931828-C-A

37357868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44931956-T-C

37358032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44932087-T-C

http://identifiers.org/hco/9/GRCh38#37358089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26209
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#44932143-A-C