http://identifiers.org/hco/5/GRCh38#36098871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9202244-C-A

36099905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9201241-G-A

36099905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9201241-G-T

36099930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9201216-A-G

36099934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9201212-A-G

36099934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9201212-A-T

36099999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9201175-G-A

36099999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9201175-G-T

36100045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9201140-G-A

36100045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9201140-G-T

http://identifiers.org/hco/5/GRCh38#36100231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9200804-A-C

36100231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200804-A-G

36100394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200642-G-A

36100419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200617-G-T

36100440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200600-G-A

36100465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200578-T-G

36100513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200530-A-G

36100522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200521-G-T

36100626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200419-T-C

36100668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200378-G-A

36100695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200351-T-C

36100708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200329-T-C

36100709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200328-A-G

36100743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9200294-C-T

http://identifiers.org/hco/5/GRCh38#36101205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9199845-C-A

36101300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9199745-G-A

36101300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9199745-G-T

36101870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9199071-C-T

36102061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9198890-C-T

36102120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9198844-G-A

36102474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9198438-G-A

36102474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9198438-G-T

36102482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9198430-G-T

36102532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9198377-A-G

http://identifiers.org/hco/5/GRCh38#36102847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9198183-C-A

36102854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9198176-T-C

36102856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9198174-T-C

36102858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9198172-G-A

36102858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9198172-G-T

36102906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9198138-C-G

36103187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9197833-G-T

36103508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9197312-T-C

36103591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9197229-C-T

36103887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9196961-T-C

http://identifiers.org/hco/5/GRCh38#36103910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9196938-A-C

http://identifiers.org/hco/5/GRCh38#36103924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9196924-C-A

36103924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 3 prime UTR variant
orthologous variants: 9196924-C-T

36104553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9195839-G-C

36104824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9195587-C-T

http://identifiers.org/hco/5/GRCh38#36105046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9194907-A-C

36105055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9194899-A-G

36105234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9194723-T-A

36105334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9194640-G-A

36105334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9194640-G-C

36105334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9194640-G-T

http://identifiers.org/hco/5/GRCh38#36105580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9194419-A-C

36105664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9194322-C-T

36105779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9194221-T-G

36105867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9194137-G-A

36105867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9194137-G-C

36106964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9188128-C-G

36107071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9188029-T-C

36107139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9187962-T-C

36107186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9187916-T-C

36107398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9187760-T-C

36107702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9187488-C-T

36107759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9187463-T-G

36107972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9187263-T-G

36107991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9187233-T-C

36108018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9187206-G-T

36108155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9187072-T-C

36108210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9187024-T-C

http://identifiers.org/hco/5/GRCh38#36108248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9186982-C-A

36108248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9186982-C-T

36108263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9186967-T-A

36108306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9186951-G-C

36108372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9186919-C-T

http://identifiers.org/hco/5/GRCh38#36108382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9186909-C-A

http://identifiers.org/hco/5/GRCh38#36108486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9186834-A-C

36108486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9186834-A-G

36108510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9186810-T-A

36108581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9186739-T-A

36108581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9186739-T-C

36108581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9186739-T-G

36108614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9186706-T-C

http://identifiers.org/hco/5/GRCh38#36108652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9186668-C-A

36108652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9186668-C-T

36108672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9186654-A-G

36109644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9184496-G-A

36109917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9184076-A-G

36109917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9184076-A-T

36109933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9184053-T-C

36110049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9183936-C-T

36110807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9183354-C-G

36110807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9183354-C-T

36110808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9183353-G-A

36111009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9182800-T-C

http://identifiers.org/hco/5/GRCh38#36111083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9182745-A-C

36111083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9182745-A-G

36111267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9182561-A-T

36111318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9182512-G-A

36111318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9182512-G-T

http://identifiers.org/hco/5/GRCh38#36111626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9181779-C-A

http://identifiers.org/hco/5/GRCh38#36112899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9180091-C-A

36112908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9180082-T-C

36114309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9178570-T-C

36114344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9178533-A-G

http://identifiers.org/hco/5/GRCh38#36114397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9178471-A-C

http://identifiers.org/hco/5/GRCh38#36114559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9178313-C-A

36114559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9178313-C-T

36114574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9178295-T-C

36114574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9178295-T-G

http://identifiers.org/hco/5/GRCh38#36114644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9178226-A-C

36114644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9178226-A-T

36114836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9178024-A-G

36114867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9177990-G-T

36114872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9177985-T-C

36114876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9177981-A-T

36114896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9177960-G-T

36115163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9177692-G-A

36115163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9177692-G-T

http://identifiers.org/hco/5/GRCh38#36115185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9177670-C-A

36115185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9177670-C-T

36115251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9177579-T-A

36115251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9177579-T-C

36116611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9175854-C-G

36116611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9175854-C-T

36116672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9175801-A-G

36117588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9175525-A-T

http://identifiers.org/hco/5/GRCh38#36117618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9175506-C-A

36117618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9175506-C-T

36117693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9175430-A-G

36118060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9175082-A-T

36118200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9174939-A-T

36118369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9174745-T-A

36118713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9174462-T-C

36119412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9174065-A-T

36122135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9172824-G-A

http://identifiers.org/hco/5/GRCh38#36122197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9172761-C-A

http://identifiers.org/hco/5/GRCh38#36122772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9171379-C-A

36122885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: missense variant
orthologous variants: 9171258-T-C

http://identifiers.org/hco/5/GRCh38#36122891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9171252-C-A

36122891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: missense variant
orthologous variants: 9171252-C-T

36123042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9171114-C-G

36123042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9171114-C-T

36123411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9170580-T-C

36123908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9166256-T-C

http://identifiers.org/hco/5/GRCh38#36124099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9166050-C-A

36124099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9166050-C-T

36124137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9166005-T-A

36124137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9166005-T-C

http://identifiers.org/hco/5/GRCh38#36124160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9165982-C-A

36124160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9165982-C-T

36124316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9165826-T-C

36125382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9160774-T-C

36125635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9160546-G-T

36125899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9160284-G-T

36125987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9160205-A-G

36126009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9160181-G-A

http://identifiers.org/hco/5/GRCh38#36126127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9160074-A-C

36126159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9159912-G-A

36126306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9159714-T-A

36136313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 9157504-A-G

36136541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9157140-T-C

36136541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9157140-T-G

http://identifiers.org/hco/5/GRCh38#36136542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9157139-A-C

36136543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9157138-A-G

36136544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9157137-T-C

36136545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9157136-A-G

36136546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9157135-T-C

36136546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9157135-T-G

36136753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9156913-T-C

36137251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9156481-G-T

http://identifiers.org/hco/5/GRCh38#36137602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9156138-C-A

36137602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9156138-C-G

36137790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9155603-G-A

36137925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9155111-C-T

http://identifiers.org/hco/5/GRCh38#36138015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9155023-A-C

36138198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9154831-A-G

36138455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9154499-T-C

http://identifiers.org/hco/5/GRCh38#36138457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9154497-C-A

36141102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9151669-C-T

36141228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151543-C-T

36141300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151474-T-G

36141425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151364-T-G

36141582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151193-T-A

36141618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151157-G-A

36141651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151121-G-A

36141709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151073-T-C

36141712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9151070-T-C

36142423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9149710-T-A

36142474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9149671-T-C

36142474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9149671-T-G

36142520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9149619-G-A

36142520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9149619-G-T

36142627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9149512-A-G

36142634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9149505-T-A

36142634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9149505-T-C

36142643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9149496-T-C

http://identifiers.org/hco/5/GRCh38#36143123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9149347-C-A

36143123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9149347-C-T

36143160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9149306-A-G

36143409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 9149057-A-G

36143496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9148976-C-T

http://identifiers.org/hco/5/GRCh38#36143500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9148972-A-C

36143533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9148936-T-C

http://identifiers.org/hco/5/GRCh38#36143537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#9148932-A-C

36143537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9148932-A-T

36147864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9144151-A-G

36147934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9144085-G-A

36147934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9144085-G-T

36148469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9143777-T-C

36148545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9143695-T-C

36148763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9143512-C-T

36148797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9143478-A-G

36148808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9143467-A-G

36150535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9141928-G-A

36150748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9141729-C-G

36151073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9141424-G-A

36151073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron variant
orthologous variants: 9141424-G-C

36151080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 9141417-C-T

36151354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9141215-C-T

36151401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 9141169-C-T

http://identifiers.org/hco/5/GRCh38#36151553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#9140976-C-A

36151627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 5 prime UTR variant
orthologous variants: 9140922-G-A

36151634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 5 prime UTR variant
orthologous variants: 9140915-C-T

36151720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 9140820-G-A

36151720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 9140820-G-T

http://identifiers.org/hco/5/GRCh38#36151759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#9140779-C-A

36151759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 9140779-C-T

36151760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25287
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 9140778-G-T