104489580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 39734337-C-T

104489892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 39734646-A-G

104490077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 39734831-G-A

104490077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 39734831-G-T

http://identifiers.org/hco/8/GRCh38#104490116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39734870-A-C

104490135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 39734876-A-G

104490135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 39734876-A-T

104490149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 39734890-T-A

http://identifiers.org/hco/8/GRCh38#104490392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39735124-C-A

104490392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 39735124-C-G

104490479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 39735227-A-T

http://identifiers.org/hco/8/GRCh38#104490694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39735432-A-C

104490694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39735432-A-G

104490697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39735435-A-G

104490712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39735450-T-C

http://identifiers.org/hco/8/GRCh38#104490722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39735460-A-C

104490789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 39735527-G-A

104490789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39735527-G-C

104491041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39735779-G-A

104491152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39735887-G-C

104491207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39735942-T-C

http://identifiers.org/hco/8/GRCh38#104491241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39735976-A-C

104491241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39735976-A-G

104491387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39736122-T-C

104491553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39736288-A-G

104491565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39736297-G-A

104491565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39736297-G-T

104491822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39736462-C-T

104492001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39736602-A-G

104492094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39736694-T-G

104492236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39736794-T-C

104492307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39736904-G-A

104492685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39737388-A-G

104492705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39737399-G-A

104493061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39737673-T-C

104493554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39738119-C-T

104493629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39738200-T-C

104493939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39738441-G-A

104494422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39738876-A-G

104494607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39739044-C-G

104494682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39739119-G-A

104494907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39739329-T-C

104494945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39739364-T-C

104494998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39739419-G-T

104495017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39739438-A-G

104495244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39739645-G-A

104495244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39739645-G-C

104495274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39739668-T-G

http://identifiers.org/hco/8/GRCh38#104495343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39739708-A-C

104495343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39739708-A-G

104495349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39739714-T-C

http://identifiers.org/hco/8/GRCh38#104495503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39739861-A-C

104495718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39739958-T-C

104495964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39740018-T-A

http://identifiers.org/hco/8/GRCh38#104496308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39740346-C-A

104496308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron variant
orthologous variants: 39740346-C-T

104496511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron variant
orthologous variants: 39740520-T-C

104496755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron variant
orthologous variants: 39740722-A-G

104496821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron variant
orthologous variants: 39740792-T-A

104496821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron variant
orthologous variants: 39740792-T-C

104496821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron variant
orthologous variants: 39740792-T-G

104496831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron variant
orthologous variants: 39740802-T-C

104496860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron variant
orthologous variants: 39740826-C-T

104496933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron variant
orthologous variants: 39741156-G-A

104497118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: synonymous variant
orthologous variants: 39741337-A-G

104497769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39741988-T-C

104497947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39742166-T-G

104497997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39742216-A-G

104498030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39742249-A-T

104498059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39742278-T-C

104498065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39742284-C-T

104498080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 39742299-T-C

104498154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39742358-G-T

104498188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39742391-T-A

104498190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39742393-C-T

104498193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39742396-G-C

104498193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39742396-G-T

104498207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39742410-C-T

104498265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39742477-G-A

104498714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39742941-T-C

104498909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39743107-T-C

104498942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39743137-T-A

104498973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39743167-T-C

http://identifiers.org/hco/8/GRCh38#104499296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39743495-C-A

104499307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39743506-A-T

104499354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39743553-G-A

104499470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39743669-A-G

104499533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39743735-C-T

104499553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39743753-T-A

104499569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39743767-A-T

104499652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39743835-C-T

104499847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39744021-T-C

http://identifiers.org/hco/8/GRCh38#104499848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39744022-A-C

104500125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39744267-G-A

104500404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39744502-G-C

104506931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39745861-T-G

104507009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39745934-T-C

104507009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39745934-T-G

104507158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39746082-A-G

104507158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39746082-A-T

104507381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39746287-T-C

104507411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39746316-G-A

http://identifiers.org/hco/8/GRCh38#104507501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39746651-A-C

104507531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39746679-G-T

104507814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39746891-A-G

104507906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39746981-T-C

http://identifiers.org/hco/8/GRCh38#104508047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39747091-C-A

104508047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39747091-C-G

104508047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39747091-C-T

104508138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39747137-T-C

http://identifiers.org/hco/8/GRCh38#104508139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39747138-C-A

104508728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39748219-A-T

http://identifiers.org/hco/8/GRCh38#104508738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39748229-C-A

104508738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39748229-C-T

104508744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39748235-T-C

104508797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39748284-G-A

104508797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39748284-G-T

104508822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39748308-T-G

104509193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39748641-T-C

104509203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39748650-T-C

104510320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39749383-T-A

104510363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39749426-A-G

104510570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39749579-C-T

104510571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39749580-G-A

http://identifiers.org/hco/8/GRCh38#104510980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39750026-C-A

104510980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39750026-C-T

104511590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39750130-A-G

104511669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39750209-T-A

104511774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39750289-G-A

104512260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39750549-T-G

104512841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39751098-T-A

104512993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39751220-T-A

104513432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39751775-A-G

104513797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39752110-G-C

104515146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39753116-C-G

104515450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39753395-T-C

104515554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39753481-G-C

104515709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39753642-C-T

104516643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39754676-G-C

104516982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39755040-G-T

104517142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39755185-T-C

http://identifiers.org/hco/8/GRCh38#104519893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39756716-A-C

104519893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39756716-A-G

104519948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39756771-T-C

104520030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39756856-G-A

104520099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39756903-G-C

104521620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39758353-T-A

104521620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39758353-T-C

104521852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39758566-A-G

104522019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39758712-T-C

104522047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39758740-T-C

104522462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39759165-G-A

104522484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39759182-A-G

104522516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39759212-C-T

104522586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39759281-G-T

104522632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39759327-T-C

104522718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39759426-T-C

104522903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39759597-T-C

104522903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39759597-T-G

104522977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39759679-C-T

104523068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39759715-A-G

104523068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39759715-A-T

104524732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39760777-G-A

104524890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39760946-G-C

104525182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39761247-A-G

104525182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39761247-A-T

104525299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39761351-C-T

104525489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39761505-T-C

104525621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39761638-T-A

104527947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39762155-C-T

104528008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39762217-A-G

http://identifiers.org/hco/8/GRCh38#104528014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39762223-A-C

104528102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39762287-G-T

104528141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39762310-G-A

http://identifiers.org/hco/8/GRCh38#104528178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39762336-C-A

104528178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39762336-C-T

104528412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39762543-G-C

104529145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39763095-G-A

104529503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39763421-T-C

104530083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39763974-T-C

104530128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39764013-T-C

http://identifiers.org/hco/8/GRCh38#104530166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39764056-A-C

104530205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39764095-T-A

104530577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39766571-C-T

104530770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39766737-G-C

104530899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39766987-G-C

104530930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39767017-G-A

104530930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39767017-G-C

104530972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39767056-G-A

104530983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39767061-T-C

104531030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39767100-T-A

104531030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39767100-T-C

104531490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39767547-T-C

104531709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39767751-T-C

104532372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39768344-T-A

104532372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39768344-T-C

104532546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39768582-A-G

104532546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39768582-A-T

104532728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39768733-G-A

104532982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39768853-G-C

104533020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39768893-T-C

104533024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39768897-A-G

104533346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39769160-C-T

104533413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39769226-C-G

104533648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39769340-A-G

104533648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39769340-A-T

104534015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39769521-T-G

104534110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39769597-G-A

104534284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39769757-C-T

104534328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39769797-C-T

104536437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39770092-G-T

104536577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39770276-G-A

104537007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39770582-G-T

104537038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39770609-G-A

http://identifiers.org/hco/8/GRCh38#104537055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39770626-C-A

104537089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39770656-T-A

http://identifiers.org/hco/8/GRCh38#104537205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#39770766-A-C

104537570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39771062-T-C

104537570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39771062-T-G

104537673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39771136-A-G

104537964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39771277-C-T

104538125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39771401-G-A

104538311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39771564-T-A

104538572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39771721-G-A

http://identifiers.org/hco/8/GRCh38#104538614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39771753-A-C

104538900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39772017-G-A

104539069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39772140-G-A

104539095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39772151-G-A

104539766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39776551-C-G

104540014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39776791-T-C

http://identifiers.org/hco/8/GRCh38#104540050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39776823-C-A

104540050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39776823-C-G

104540207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39776950-T-G

104540362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39777081-G-A

104541160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39777925-T-C

104550392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39785457-A-T

104550410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39785467-T-C

104550410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39785467-T-G

104550683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39785702-T-A

104550769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39785788-T-C

104550945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39785948-G-A

104551128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39786095-T-C

104551297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39786238-G-A

104551297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39786238-G-T

104551305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39786246-A-T

104551845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39786380-C-T

104551927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39786452-T-C

104560067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39787955-T-C

http://identifiers.org/hco/8/GRCh38#104560137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39788022-A-C

104560198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39788075-T-C

104560422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39788253-A-T

104560432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39788263-T-C

104560500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39788310-C-T

http://identifiers.org/hco/8/GRCh38#104560661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39788437-A-C

104560927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39788864-G-A

104560975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39788911-T-C

104561783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39789343-T-C

104562465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39789981-G-A

104562524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39790038-T-C

104562634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39790180-G-A

104562635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39790181-G-T

104562661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39790199-G-A

http://identifiers.org/hco/8/GRCh38#104562909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39790445-A-C

104563008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39790548-A-G

104572361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39797080-C-G

104572371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39797090-A-G

http://identifiers.org/hco/8/GRCh38#104572372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39797091-C-A

104572722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39797388-G-A

104572746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39797403-G-A

104572791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39797464-C-G

104572866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39797534-C-T

104573063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39797896-T-C

104573338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39798138-G-A

104573588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39798348-G-A

104573588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39798348-G-T

http://identifiers.org/hco/8/GRCh38#104573717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39798459-C-A

104573723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39798465-T-C

104573740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39798481-G-A

104574682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39799339-A-G

http://identifiers.org/hco/8/GRCh38#104574935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39799590-A-C

104574957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39799612-A-G

104575029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39799677-A-G

104581764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39800117-C-G

104581830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39800174-G-T

http://identifiers.org/hco/8/GRCh38#104582164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39800455-A-C

104582170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39800461-A-G

http://identifiers.org/hco/8/GRCh38#104582626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39800896-A-C

104582826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801117-T-C

104583217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801497-A-G

104583276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801552-T-C

104583316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801587-T-C

http://identifiers.org/hco/8/GRCh38#104583358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39801608-C-A

104583358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801608-C-T

104583375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801624-T-C

104583392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801642-G-A

104583392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801642-G-T

104583439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801688-T-C

104583448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801697-T-C

104583520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801762-A-G

104583522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801764-G-A

104583559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801801-T-G

104583671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39801889-G-C

http://identifiers.org/hco/8/GRCh38#104583818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39802013-C-A

104583883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802051-G-C

104583883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802051-G-T

104583960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802128-T-C

104583989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802157-A-G

104584002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802170-C-T

104584099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802226-A-G

104584104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802230-G-A

104584104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802230-G-C

104584130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802255-A-G

104584233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802336-C-T

104584367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802472-G-T

104584448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802558-A-G

104584493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39802721-C-G

104584915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39803134-T-G

104584975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39803198-T-C

104584975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39803198-T-G

http://identifiers.org/hco/8/GRCh38#104586109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39803741-A-C

104586145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39803776-T-G

104586174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39803817-T-C

104586197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39803855-A-T

104586473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39804184-T-C

104586609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39804722-C-T

104586775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39804950-T-C

104586807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39804981-T-G

104587059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39805201-C-T

104587150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39805287-G-A

104587251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39805392-T-C

104587420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39805546-A-G

104587730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39805859-C-G

104587730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39805859-C-T

104587913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806133-C-G

104587925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806147-G-A

104587925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806147-G-C

104588087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806287-C-T

104588107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806307-T-C

104588118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806318-G-C

104588138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806337-T-G

104588316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806516-G-A

http://identifiers.org/hco/8/GRCh38#104588419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39806614-C-A

104588419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806614-C-T

http://identifiers.org/hco/8/GRCh38#104588496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39806686-C-A

104588500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806690-T-C

104588500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806690-T-G

http://identifiers.org/hco/8/GRCh38#104588548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39806737-C-A

104588548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806737-C-T

104588635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806818-T-G

104588713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806892-A-G

http://identifiers.org/hco/8/GRCh38#104588744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39806921-C-A

104588744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39806921-C-T

http://identifiers.org/hco/8/GRCh38#104588855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39807036-A-C

104588855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39807036-A-G

104588872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39807053-T-A

104588872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39807053-T-G

http://identifiers.org/hco/8/GRCh38#104589009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39807156-C-A

104589009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 39807156-C-T

104589182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31708
most severe consequence: 5 prime UTR variant
orthologous variants: 39807300-G-C