36296342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101713346-C-T

36296404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101713284-G-T

36296413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101713275-T-C

36296414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101713274-G-A

36296414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101713274-G-T

36296450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101713240-G-A

36296543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101713165-G-A

36296543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101713165-G-T

36296710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101712454-A-T

36296769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101712396-A-G

36296776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101712389-C-T

36297211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101711977-C-G

36297244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101711943-T-C

http://identifiers.org/hco/11/GRCh38#36297246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101711941-C-A

http://identifiers.org/hco/11/GRCh38#36297277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101711904-C-A

36297278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101711903-A-G

http://identifiers.org/hco/11/GRCh38#36297403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101711788-C-A

36297403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101711788-C-G

36297470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101711731-A-G

36297494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101711710-A-G

36299285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101708083-T-C

36299289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101708079-G-A

36299467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101707917-G-A

36299492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101707892-C-T

36299604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101707788-T-C

36300052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101707364-C-G

36300052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101707364-C-T

36301108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101706066-T-A

36301108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101706066-T-C

36301296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101705918-T-G

36301304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101705902-G-C

36301352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101705853-C-T

36301441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101705789-G-A

36301871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101705277-G-A

36301963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101705189-A-G

36302049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101705106-G-C

36302137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101705065-C-G

36302137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101705065-C-T

http://identifiers.org/hco/11/GRCh38#36302176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101705030-A-C

36302258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704961-A-G

36302427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704799-A-G

36302904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704585-A-G

36302982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704508-C-G

36302982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704508-C-T

36303119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704375-G-C

36303127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704367-C-T

36303195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704304-G-C

36303217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704282-G-A

36303295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704220-G-A

36303295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704220-G-C

http://identifiers.org/hco/11/GRCh38#36303348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101704167-C-A

36303348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704167-C-T

36303381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101704134-A-G

36303543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101703971-T-C

http://identifiers.org/hco/11/GRCh38#36303663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101703851-A-C

36303663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101703851-A-T

36303744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101703772-A-G

36303977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101703555-C-T

36304038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101703502-T-A

36304041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101703499-G-A

36304067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101703475-C-T

36304071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101703471-G-A

36304109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101703433-T-C

36304179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101703350-G-A

36304430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101702833-G-T

36304536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101702726-G-C

http://identifiers.org/hco/11/GRCh38#36308637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101700323-A-C

36308637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101700323-A-G

36308845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101700156-G-A

36308883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101700118-C-T

36309011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101699485-G-T

36309055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101699450-G-A

36309071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101699429-A-G

36309257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101699271-A-G

36309581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101698990-T-A

36309583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101698988-C-T

36309739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101698749-A-G

36310202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101698158-G-A

36311085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101697069-A-G

36311119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101697039-A-T

36311361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101696835-C-T

36311424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101696773-A-G

36311436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101696763-C-T

36311515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101696689-A-G

36311647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101696572-A-T

36311658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101696559-A-G

36311706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101696465-T-A

36311834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101696336-C-T

http://identifiers.org/hco/11/GRCh38#36312151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101695507-C-A

36312199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101695451-T-A

36312245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101695361-A-G

36312325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101695288-G-C

36312361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101695252-G-A

36312361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101695252-G-C

36312473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101695163-G-A

36312764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101694895-C-T

36312984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101694675-G-A

36313095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101694559-A-G

36313183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101694474-A-G

36313296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101694369-G-A

36313396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101694272-A-G

36313400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101694268-G-A

36313475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101693967-T-G

36313682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101693764-A-T

36313693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101693754-G-A

36313730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101693717-G-A

36313730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101693717-G-C

36313990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101693495-A-T

36314002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101693483-T-A

36314311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101693171-A-G

36314377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101693098-C-G

36315006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101692286-A-G

36315046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101692246-A-G

36315308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101692004-A-G

36315776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101691523-G-T

36315987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101691313-A-G

36315987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101691313-A-T

36317236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101690751-T-C

36317238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101690749-A-T

36317273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101690717-A-G

36317283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101690707-C-T

36317708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101690292-G-T

36318698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101689697-G-T

http://identifiers.org/hco/11/GRCh38#36318712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101689686-C-A

36318712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101689686-C-T

36318713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101689685-G-A

36318990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101689402-C-T

36319043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101689351-G-C

36319114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101688890-C-G

36319703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101685842-A-G

36319703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101685842-A-T

36319766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101685805-C-T

36319790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101685782-G-A

36320071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101685547-A-G

36320447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101685365-T-C

36320560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101685255-T-C

36320646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101685163-T-A

36320754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101685073-C-T

36321150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101684709-C-T

http://identifiers.org/hco/11/GRCh38#36321208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101684648-C-A

36321208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101684648-C-T

36321267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101684601-G-T

36321268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101684600-A-G

36321292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101684577-A-T

36321293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101684576-A-G

http://identifiers.org/hco/11/GRCh38#36321325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101684544-C-A

36321325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101684544-C-G

36321325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101684544-C-T

36321345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101684528-C-T

36321383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101684488-T-C

36321454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101684417-G-A

36321454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101684417-G-T

36321459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101684412-G-C

36321613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101684294-A-T

36321646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101684264-G-A

http://identifiers.org/hco/11/GRCh38#36321670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101684240-C-A

36321670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101684240-C-T

http://identifiers.org/hco/11/GRCh38#36321727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101684175-C-A

36321850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101684037-C-T

36321947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101683966-C-T

36321987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101683926-C-G

36322129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101683683-A-G

36322419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101683210-C-G

36322419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101683210-C-T

36322453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101683172-G-T

36322627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101683002-C-T

http://identifiers.org/hco/11/GRCh38#36322677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101682969-C-A

36322677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101682969-C-T

http://identifiers.org/hco/11/GRCh38#36323202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101679515-C-A

36323202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101679515-C-T

36323214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101679505-G-T

36323234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101679485-G-C

36323234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101679485-G-T

36323270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101679449-G-T

36323387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101679348-G-A

36323387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101679348-G-T

36323477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101679287-G-A

http://identifiers.org/hco/11/GRCh38#36323564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101679208-C-A

36323599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101679169-G-C

36323703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101679066-A-G

36324410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101678533-T-C

36324432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101678511-G-T

http://identifiers.org/hco/11/GRCh38#36328595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101675893-C-A

36328700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101675794-G-C

36328949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101675546-C-T

36329071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101675460-T-C

36329208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101675353-G-A

36329272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101675299-C-T

36329281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101675286-T-C

36329375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101675200-G-A

36329389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101675186-A-G

http://identifiers.org/hco/11/GRCh38#36329414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101675163-A-C

36329443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101675134-T-C

36329682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101674891-A-T

36335459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101668537-G-T

36335468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101668528-A-T

36335534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101668462-C-G

36335753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101668213-A-G

36335842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101668125-G-A

36335864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101668111-C-T

36339744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101663657-G-A

36339761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101663640-C-T

36339762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101663639-A-G

36339828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101663589-C-G

36339828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101663589-C-T

http://identifiers.org/hco/11/GRCh38#36339830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101663587-C-A

36340179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101663059-C-T

http://identifiers.org/hco/11/GRCh38#36340364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101662883-C-A

36340546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101662752-A-G

36340886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101662411-C-T

36340989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101662318-C-T

36341096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101662214-G-A

36341233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101662088-G-T

36341234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101662087-C-T

36342797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101660876-C-T

36344768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101658667-G-C

36345130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101658287-G-A

36345134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101658283-T-G

36345396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101658046-G-A

36345560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101657919-A-G

http://identifiers.org/hco/11/GRCh38#36345897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101657648-A-C

36345991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101657568-T-G

36346473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101657126-C-T

36346482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101657117-T-C

36346885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101656816-T-C

36346892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101656809-C-G

36346992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101656718-A-G

36347077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101656599-T-C

36347190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101656493-T-G

36347364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101656318-G-A

36347717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101655664-T-C

36347843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101655547-A-G

36347847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101655543-G-T

36347883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101655507-G-C

36347884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101655506-A-G

http://identifiers.org/hco/11/GRCh38#36347902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101655488-C-A

36347902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101655488-C-T

36347956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101655393-C-T

36347957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101655392-C-G

36348109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101655131-T-A

36348111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101655129-T-G

36348153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101655101-C-T

36348230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101655038-A-G

36348294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101654976-C-T

36348301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101654969-T-C

36348304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101654966-A-G

36348354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101654922-A-G

36348422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101654887-C-T

36349292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101653597-A-G

36354422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101650081-G-A

36356416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101649368-T-C

36358960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101649034-T-C

36358961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101649033-A-G

36359284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101648760-T-A

36361406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101646662-A-T

36361743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101646305-T-G

36361809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101646200-A-G

36361871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101646138-C-G

36361871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101646138-C-T

36362019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101646008-G-A

36362019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101646008-G-C

36362033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101645996-T-A

36362057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101645974-G-A

36362057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101645974-G-T

36362095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101645925-G-A

36362210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101645838-A-T

36362228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101645820-T-C

36362228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101645820-T-G

http://identifiers.org/hco/11/GRCh38#36362280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101645769-C-A

http://identifiers.org/hco/11/GRCh38#36362314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101645737-C-A

36362445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101645596-C-G

36362445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101645596-C-T

36362556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101645524-A-T

36362782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101645319-T-C

36363387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101644528-C-G

36363575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101644356-T-C

36363787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101644164-C-T

36363873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101644075-A-G

36363937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101644020-C-T

36364444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101642934-G-A

36364533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101642849-A-G

36364836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101642427-T-G

36364884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101642379-C-T

36365237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101642034-G-C

36365399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101641861-C-T

http://identifiers.org/hco/11/GRCh38#36365404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101641856-A-C

36365433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101641829-C-T

36365440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101641822-A-T

36365507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101641765-A-T

36365531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101641740-C-G

36365958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101641102-C-G

36366076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101640989-T-G

36366205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101640851-T-C

36366248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101640804-C-G

36366304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101640755-C-T

36366394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101640677-A-G

36367181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101639357-A-G

36367181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101639357-A-T

36368091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101638660-T-A

36368185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101638571-T-C

36368185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101638571-T-G

36368318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101638441-A-G

http://identifiers.org/hco/11/GRCh38#36368329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101638429-A-C

36368329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101638429-A-G

36368348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101638410-G-A

36368439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101638321-G-A

36368562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101638200-A-G

36368628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101638136-C-T

36368637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101638127-C-T

36368729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101637916-C-T

36368815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101637841-T-C

36368818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101637838-T-C

36369264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101637448-A-G

36371376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101632785-T-G

36371434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101632730-T-A

36371434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101632730-T-C

36371462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101632702-C-T

36371513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101632656-G-A

36372558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101631842-C-T

36372589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101631812-C-T

http://identifiers.org/hco/11/GRCh38#36372906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101631510-C-A

36373566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101630896-T-A

36373691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101630787-T-G

36373708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101630770-T-C

http://identifiers.org/hco/11/GRCh38#36373847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101630629-C-A

36374362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101630264-G-A

36374549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101630216-A-G

36374647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101630156-G-A

36374882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101629940-G-A

36375260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101629701-C-T

36375332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101629632-C-T

36375368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101629619-C-T

36375423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101629571-C-T

36375457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101629537-C-T

http://identifiers.org/hco/11/GRCh38#36375986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101628353-C-A

36375986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101628353-C-T

36375990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101628345-G-A

36375990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101628345-G-T

36376016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101628333-G-A

36376016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101628333-G-T

36376035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101628314-T-C

36376056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101628293-G-A

36376056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101628293-G-T

36376182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101628178-G-A

http://identifiers.org/hco/11/GRCh38#36376300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101628078-A-C

36376300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101628078-A-G

36376300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101628078-A-T

36376301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101628077-G-T

36376303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101628075-A-G

36376303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101628075-A-T

36376402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101628030-A-G

36376518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101627941-A-G

36376518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101627941-A-T

36376524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101627935-G-A

36376524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101627935-G-C

36376524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101627935-G-T

36376533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101627926-G-A

36376533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101627926-G-C

36376533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101627926-G-T

36376588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101627884-G-T

36376628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 101627844-G-T

http://identifiers.org/hco/11/GRCh38#36376640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101627832-C-A

36376672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101627800-C-T

36377025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101627485-G-A

36377081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101627440-T-C

36377200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101627323-A-G

36377436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101627112-G-A

36377436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101627112-G-C

http://identifiers.org/hco/11/GRCh38#36377502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101627065-C-A

36377502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101627065-C-T

http://identifiers.org/hco/11/GRCh38#36377507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101627060-C-A

36377507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101627060-C-T

http://identifiers.org/hco/11/GRCh38#36377515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101627052-C-A

36377515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101627052-C-T

36377603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101626968-T-A

36377603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101626968-T-C

http://identifiers.org/hco/11/GRCh38#36377606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101626965-C-A

36377606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101626965-C-T

36377683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101626888-G-A

36377683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101626888-G-T

36377696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101626875-C-T

http://identifiers.org/hco/11/GRCh38#36377723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101626848-C-A

36377723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 101626848-C-T

36377784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101626782-G-A

36377811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101626755-G-A

36377811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101626755-G-T

http://identifiers.org/hco/11/GRCh38#36377847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101626719-C-A

36377847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101626719-C-T

36378047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101626547-C-T

http://identifiers.org/hco/11/GRCh38#36378069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101626531-A-C

36378111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101626503-C-T

36378135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101626482-T-C

36378188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101626428-T-C

36378250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101626382-C-T

36378435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101626248-A-G

36378435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101626248-A-T

36378479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101626213-G-A

36378479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101626213-G-C

36378648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101626056-G-A

36378648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101626056-G-C

36379037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101625385-A-G

36379045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101625377-A-G

36379183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101625242-G-C

36379277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101625153-G-A

36379293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101625141-T-C

36379317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101625108-C-T

36379351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101625073-C-T

36379481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101624947-A-G

36379691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101624746-G-A

36379691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101624746-G-C

http://identifiers.org/hco/11/GRCh38#36380388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101623769-C-A

36380388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101623769-C-T

36380927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101623193-A-G

36381098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101623038-C-T

36381103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101623033-A-G

36381572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101622693-G-A

36381572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101622693-G-T

http://identifiers.org/hco/11/GRCh38#36381584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101622681-A-C

36381603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101622661-A-G

36381635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101622628-C-T

36381646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101622617-T-C

http://identifiers.org/hco/11/GRCh38#36381714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101622550-C-A

36381801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101622474-T-G

36381802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101622473-T-C

36383004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101619986-G-C

36383022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101619968-A-G

36383033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101619957-T-G

36383136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101619898-G-A

36383193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101619841-C-T

36383346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101619684-C-G

36383705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101619381-T-C

36383720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101619366-G-C

36383959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101619086-T-C

36384314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101618642-A-G

36384488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101618441-T-C

36385255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101618072-C-T

36385508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101617796-A-G

36385619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101617693-C-T

http://identifiers.org/hco/11/GRCh38#36385904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101617568-C-A

36386183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101617438-A-T

36386273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101617396-G-A

36386296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101617375-A-T

36386498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101617271-T-A

36386498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101617271-T-C

36386558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101617258-G-T

36386559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 101617257-G-T

36386654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101617190-G-T

36386656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101617188-G-A

36386776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101617068-A-T

36386808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101617018-T-C

36391284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101611695-A-G

36391419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101611343-T-C

36391561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101611200-A-G

36393864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101610936-A-G

36393925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101610890-G-T

36393935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101610880-T-C

36393936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101610879-G-A

36393936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101610879-G-T

36393969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101610846-A-G

36394012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 101610803-G-A

36394035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101610780-G-T

36394049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101610766-C-T

http://identifiers.org/hco/11/GRCh38#36394068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101610747-C-A

http://identifiers.org/hco/11/GRCh38#36394087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101610728-C-A

36394087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101610728-C-T

36394116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101610699-G-C

36394125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101610690-G-A

http://identifiers.org/hco/11/GRCh38#36394213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101610528-C-A

36394223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101610512-A-G

36394416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101610236-A-G

36394452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101610199-T-C

36394523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101610128-T-C

36394733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101609917-C-T

36394972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101609568-C-T

36395219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101609362-A-G

36395305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101609287-G-A

36396309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606520-T-C

36396328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606539-G-T

36396355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606560-G-A

36396494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606706-C-T

36396497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606709-C-T

36396569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606782-C-G

36396642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101607283-A-G

36396731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606444-G-T

36396752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606423-A-G

36396782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606385-T-C

36396822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606341-C-T

36396842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606320-A-G

36396852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606310-G-T

36397012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606126-A-G

36397042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101606096-T-C

36398198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605901-C-T

36398204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605895-C-T

http://identifiers.org/hco/11/GRCh38#36398316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101605799-C-A

36398326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605789-A-G

36398368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605748-T-C

http://identifiers.org/hco/11/GRCh38#36398371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101605745-C-A

36398371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605745-C-G

36398371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605745-C-T

http://identifiers.org/hco/11/GRCh38#36398379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101605737-C-A

36398379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605737-C-T

36398403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605713-G-A

36398403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605713-G-C

http://identifiers.org/hco/11/GRCh38#36398417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101605697-C-A

http://identifiers.org/hco/11/GRCh38#36398446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101605671-C-A

36398446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605671-C-T

36398454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605663-T-C

36398458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605658-T-C

36398468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605648-G-A

36398468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605648-G-T

http://identifiers.org/hco/11/GRCh38#36398516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101605619-A-C

36398726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605350-G-T

36398732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605344-G-A

36398732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605344-G-C

36398732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605344-G-T

http://identifiers.org/hco/11/GRCh38#36398753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101605323-C-A

36398753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605323-C-G

36398753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605323-C-T

http://identifiers.org/hco/11/GRCh38#36398777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101605301-C-A

36398791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605289-A-G

36398792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605288-G-T

36398814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605273-T-C

36398817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605270-G-A

36398817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 101605270-G-T

36398846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605249-C-T

36398849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605246-T-C

http://identifiers.org/hco/11/GRCh38#36398875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101605222-C-A

36398875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605222-C-T

36398888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605209-A-G

36399065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101605037-T-G

36399116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101604986-T-C

36399382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101604729-C-T

http://identifiers.org/hco/11/GRCh38#36399646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101604506-C-A

36400366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101603295-A-G

36400366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101603295-A-T

36400461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101603203-T-C

36400461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101603203-T-G

36400569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101603125-G-A

36400570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101603124-C-T

36400579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101603112-G-A

36400715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101603015-A-G

36400795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602954-T-G

http://identifiers.org/hco/11/GRCh38#36400817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101602932-C-A

36400823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602926-C-G

http://identifiers.org/hco/11/GRCh38#36400865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101602884-C-A

36400865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602884-C-T

36400916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602828-G-C

36400916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602828-G-T

36400947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602797-A-T

36400974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602773-T-C

http://identifiers.org/hco/11/GRCh38#36401043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101602715-C-A

36401043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101602715-C-T

http://identifiers.org/hco/11/GRCh38#36401048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101602710-C-A

36401048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101602710-C-G

36401048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101602710-C-T

http://identifiers.org/hco/11/GRCh38#36401128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101602630-C-A

36401128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101602630-C-T

36401155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101602603-G-A

36401215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101602543-C-G

36401215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101602543-C-T

36401325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602453-G-T

36401342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602432-G-A

36401342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602432-G-T

36401347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602427-A-G

http://identifiers.org/hco/11/GRCh38#36401350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101602424-C-A

36401350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602424-C-T

36401358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602416-G-T

http://identifiers.org/hco/11/GRCh38#36401360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101602414-C-A

36401360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602414-C-T

36401383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602391-A-G

36402076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101602048-A-G

http://identifiers.org/hco/11/GRCh38#36402134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101601991-C-A

36402134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101601991-C-G

36402783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101601725-C-T

http://identifiers.org/hco/11/GRCh38#36403120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101601534-C-A

36403120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101601534-C-T

http://identifiers.org/hco/11/GRCh38#36403122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101601532-C-A

http://identifiers.org/hco/11/GRCh38#36403212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101601445-C-A

36403212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101601445-C-T

http://identifiers.org/hco/11/GRCh38#36403273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101601384-C-A

http://identifiers.org/hco/11/GRCh38#36403305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101601351-A-C

36403462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101601228-G-A

36403462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101601228-G-T

36403583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101601096-T-C

36403597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101601081-T-C

36403742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101600942-T-C

http://identifiers.org/hco/11/GRCh38#36403774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101600918-C-A

36403774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101600918-C-T

36404047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101600452-T-C

36404728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101600123-G-T

http://identifiers.org/hco/11/GRCh38#36404852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101599983-C-A

36404852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101599983-C-G

36404883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101599952-A-G

36405429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101599271-G-T

36405522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101599186-A-G

36405711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101598992-A-G

36405744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101598959-T-C

36405782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101598928-T-G

36405880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101598829-T-C

36405903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101598802-G-A

36405978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101598753-G-T

36406189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101598567-A-G

36406192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101598564-A-G

36406737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101597726-G-T

36406819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101597644-T-C

36406859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101597607-C-G

36406859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101597607-C-T

36407029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101597468-A-G

36407162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101597348-A-G

36407166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101597344-T-A

36407266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101597313-G-A

36407780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101596416-T-A

36407780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101596416-T-C

36407946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101596262-T-C

36408333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101596198-G-T

36408472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101596059-A-G

36408930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101595769-T-G

http://identifiers.org/hco/11/GRCh38#36409172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101595564-A-C

36409214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101595533-C-G

http://identifiers.org/hco/11/GRCh38#36409227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101595520-C-A

36409335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101595416-A-G

36409397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101595358-G-C

36409629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101595145-G-A

36409629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101595145-G-T

36409770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101595000-A-G

36410724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101594540-A-G

36411484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101593591-T-G

36411825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101593271-A-G

36411887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101593213-A-G

36411975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101593119-C-G

36412016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101593086-C-T

36412308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101592823-T-A

http://identifiers.org/hco/11/GRCh38#36412341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101592795-C-A

36412502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101592643-C-G

36412533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101592609-G-A

36412669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101592470-A-G

36412922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101591458-A-T

36412966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101591404-G-A

36417480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101590418-C-T

36418091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101589823-T-C

36418727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101589321-C-T

http://identifiers.org/hco/11/GRCh38#36418814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101589235-A-C

36419323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101588833-G-A

36419366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101588793-G-A

http://identifiers.org/hco/11/GRCh38#36419394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101588767-C-A

36419394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101588767-C-G

http://identifiers.org/hco/11/GRCh38#36419418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101588738-C-A

36419418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101588738-C-G

36419467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101588714-G-A

36419467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101588714-G-T

36419600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101588579-C-T

36420698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101587355-G-A

36421048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101586904-C-T

36421067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101586885-C-T

36421158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101586769-C-T

36421203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101586724-T-G

36421254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101586674-G-A

http://identifiers.org/hco/11/GRCh38#36421517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101586405-C-A

36421885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101586114-G-A

36421915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101586084-A-G

36422362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101585703-A-G

http://identifiers.org/hco/11/GRCh38#36422381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101585680-C-A

http://identifiers.org/hco/11/GRCh38#36422417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101585650-C-A

36422654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101585374-G-A

36422880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101585144-A-G

36422890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101585134-C-G

36423082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101584940-G-A

36423082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101584940-G-C

36423332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101584651-C-T

36424095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101583953-T-C

36426943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101583326-C-G

36426943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101583326-C-T

36426990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101583266-C-G

http://identifiers.org/hco/11/GRCh38#36426992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101583264-C-A

36427106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101583144-G-T

36427192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101583059-A-G

36427227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101583035-C-T

36427234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101583028-C-T

36427395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101582862-G-A

36427612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101582642-G-A

36427612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101582642-G-C

36427899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101582423-A-G

36427945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101582395-C-T

http://identifiers.org/hco/11/GRCh38#36428335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101582211-C-A

36428623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101581846-G-C

36429145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101581398-T-C

36429505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101580660-C-T

36429891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101580222-G-A

36430038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101580113-T-G

http://identifiers.org/hco/11/GRCh38#36430975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101578357-C-A

36430975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101578357-C-G

36430984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101578344-T-C

http://identifiers.org/hco/11/GRCh38#36431347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101578012-C-A

36431354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101578006-C-G

36431390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101577973-T-C

36431612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101577396-G-A

36431618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101577387-G-C

36431714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101577293-A-G

http://identifiers.org/hco/11/GRCh38#36431774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101577236-C-A

36431774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101577236-C-T

36431826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101577153-C-T

36431834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101577145-C-G

36431883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101577096-G-A

36431916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101577063-T-A

36431916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101577063-T-C

36431981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101576997-G-T

36432001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101576977-G-A

36432001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101576977-G-T

http://identifiers.org/hco/11/GRCh38#36432021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101576957-C-A

36432021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101576957-C-G

36432021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101576957-C-T

http://identifiers.org/hco/11/GRCh38#36432037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101576941-C-A

36432037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101576941-C-T

http://identifiers.org/hco/11/GRCh38#36432079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101576913-A-C

36432494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101576541-G-T

36432559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101576495-T-G

36432581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101576473-T-A

http://identifiers.org/hco/11/GRCh38#36432666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101575888-A-C

36432747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101575822-T-A

36432757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101575808-A-G

36432798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101575766-C-G

http://identifiers.org/hco/11/GRCh38#36432871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101575655-A-C

36432955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101575561-T-C

36433044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101575472-C-T

36433934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101574731-T-C

36433934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101574731-T-G

36434127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101574527-T-C

36434237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101574411-C-G

36434533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101574164-G-A

36434533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101574164-G-T

http://identifiers.org/hco/11/GRCh38#36434570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101574135-C-A

36434957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101573790-C-T

36435459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101573395-A-G

36435459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101573395-A-T

http://identifiers.org/hco/11/GRCh38#36435814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101573022-C-A

36435814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101573022-C-T

36435827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101572999-A-T

36435955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101572877-T-C

36436108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101572780-G-A

36436109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101572779-G-T

36436313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101572576-A-G

36436313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101572576-A-T

36436447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101572476-G-A

http://identifiers.org/hco/11/GRCh38#36437242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101571854-C-A

36437242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101571854-C-G

36437253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101571844-T-A

36437266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101571831-C-T

36437291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101571806-A-G

36437293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101571804-A-G

36437294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101571803-T-G

36437315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101571782-G-A

36437315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101571782-G-T

http://identifiers.org/hco/11/GRCh38#36437468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101571638-C-A

36437468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101571638-C-G

36437488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101571618-T-G

http://identifiers.org/hco/11/GRCh38#36437511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101571611-C-A

http://identifiers.org/hco/11/GRCh38#36437534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101571588-C-A

36437625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101571500-T-C

http://identifiers.org/hco/11/GRCh38#36437956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101571034-A-C

36438155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101570601-T-A

36438202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101570544-C-G

36438328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101570423-A-T

36438329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101570422-G-A

36438335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101570416-G-A

36438342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101570409-A-G

36438344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101570407-G-T

36438457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101570298-T-C

36439286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101569421-T-C

36439367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101569340-G-A

36439394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101569313-G-C

http://identifiers.org/hco/11/GRCh38#36439471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101569279-C-A

36439471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101569279-C-T

36439512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101569247-G-C

36439571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101569192-G-A

36439878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101569032-T-C

36439898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101569012-G-C

http://identifiers.org/hco/11/GRCh38#36440052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101568902-C-A

http://identifiers.org/hco/11/GRCh38#36440131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101568836-C-A

36440165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101568800-G-A

36440296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101568691-A-G

36440297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101568690-T-C

36440308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101568685-G-A

36440308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101568685-G-C

http://identifiers.org/hco/11/GRCh38#36444330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101567586-A-C

36444578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101567219-G-A

36444743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101567041-T-C

36444969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101566838-A-T

http://identifiers.org/hco/11/GRCh38#36445707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101565682-C-A

36445887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101565491-C-T

36446097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101565281-C-T

36446105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101565273-G-A

http://identifiers.org/hco/11/GRCh38#36446194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101565191-C-A

36446194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101565191-C-T

36447270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101563973-G-T

http://identifiers.org/hco/11/GRCh38#36447354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101563878-A-C

http://identifiers.org/hco/11/GRCh38#36447682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101563700-C-A

36447682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101563700-C-G

36447685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101563697-A-G

36447793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101563599-G-C

36447867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101563542-T-C

36447893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101563518-C-T

36447906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101563505-A-T

http://identifiers.org/hco/11/GRCh38#36447923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101563488-A-C

http://identifiers.org/hco/11/GRCh38#36448203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101562928-C-A

http://identifiers.org/hco/11/GRCh38#36448380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101562780-C-A

http://identifiers.org/hco/11/GRCh38#36448526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101562656-A-C

36448773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101562447-G-A

36448851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101562371-T-C

36450006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101562067-C-G

36450154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101561931-G-A

36450270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101561833-G-T

http://identifiers.org/hco/11/GRCh38#36450391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101561720-C-A

36450820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101561240-C-G

36450820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101561240-C-T

36450864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101561188-G-A

36450866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101561186-C-T

36451061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101560034-G-A

36451111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101559985-G-A

36451111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101559985-G-T

http://identifiers.org/hco/11/GRCh38#36451165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101559934-C-A

36451320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101559782-C-T

http://identifiers.org/hco/11/GRCh38#36451428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101559702-A-C

36451428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101559702-A-G

36451429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101559701-G-A

36451462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101559671-T-A

36451743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101558986-T-C

36452037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101558686-G-A

36452176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101558541-T-C

36452179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101558538-T-C

36452182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101558535-G-A

36452360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101558351-G-A

36452360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101558351-G-C

36452636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101558078-T-G

36452639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101558075-G-A

36452825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101557857-T-G

36453838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101555553-A-T

36453868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101555524-G-A

36453868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101555524-G-T

http://identifiers.org/hco/11/GRCh38#36453879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101555513-C-A

36453899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101555495-C-T

36453980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101555411-G-A

36453980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101555411-G-T

36453994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101555397-G-A

36453994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101555397-G-T

36454009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101555383-G-T

36454021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101555371-G-A

36454021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101555371-G-T

36454159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101555301-G-A

36454159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101555301-G-C

36454159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101555301-G-T

http://identifiers.org/hco/11/GRCh38#36454238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101555229-C-A

36454238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101555229-C-T

36454246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101555221-G-T

36454962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553667-G-A

36455075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553546-A-G

36455206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553397-G-A

36455206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553397-G-T

36455239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553390-C-T

36455288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553365-T-C

36455288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553365-T-G

36455314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101553336-G-T

36455387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101553272-T-C

36455507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553196-G-T

36455514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553189-A-G

36455542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553180-G-T

36455619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553108-C-T

36455666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553061-G-A

36455666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101553061-G-C

36455882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101552920-G-T

36456216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101552588-G-A

36456216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101552588-G-T

36456331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101552490-G-T

36456349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101552489-G-C

36456376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101552462-T-C

36456639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101550981-T-G

36456953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101550703-T-G

36456954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101550702-T-C

http://identifiers.org/hco/11/GRCh38#36456981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101550632-C-A

36456981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101550632-C-G

36456981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101550632-C-T

36457708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101550165-C-T

36457754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101550121-C-T

36457893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101550004-T-C

36458212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101549741-C-T

36460715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101549493-A-G

36461143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101549098-G-A

http://identifiers.org/hco/11/GRCh38#36461393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101548863-C-A

36461393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101548863-C-T

http://identifiers.org/hco/11/GRCh38#36462045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101548086-C-A

36462244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101547899-G-A

36462244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101547899-G-C

36462244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101547899-G-T

36462255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101547892-T-C

36462287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101547868-T-G

36462298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101547857-T-C

36462304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101547847-C-G

36462304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101547847-C-T

36462312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101547839-T-A

36462422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101547729-A-G

36462464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101547687-G-A

36462488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101547663-G-A

36462488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101547663-G-C

36462492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101547659-G-A

36462656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101547495-A-G

http://identifiers.org/hco/11/GRCh38#36462665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101547486-C-A

36462665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101547486-C-G

36462665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101547486-C-T

36462736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: 101547409-A-G

36462736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: 101547409-A-T

http://identifiers.org/hco/11/GRCh38#36462747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101547398-C-A

36462747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547398-C-T

36462750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547395-G-T

36462769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547379-T-C

36462769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547379-T-G

36462770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547378-T-A

http://identifiers.org/hco/11/GRCh38#36462902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101547250-C-A

36463000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547179-C-T

http://identifiers.org/hco/11/GRCh38#36463011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101547168-A-C

36463017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547162-G-A

36463017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547162-G-T

36463035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547147-T-C

36463051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547131-G-A

36463051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547131-G-T

36463079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547109-G-A

36463079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101547109-G-T

http://identifiers.org/hco/11/GRCh38#36463128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101547069-A-C

http://identifiers.org/hco/11/GRCh38#36463155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101547043-A-C

http://identifiers.org/hco/11/GRCh38#36463241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101546975-C-A

36463400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546821-A-G

36463495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546762-G-A

36463508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546748-C-G

36463585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546681-C-T

http://identifiers.org/hco/11/GRCh38#36463764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101546510-C-A

36463912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546377-C-G

36463920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546369-G-T

36463934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546355-A-G

36463980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546320-A-G

36463986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546317-G-A

http://identifiers.org/hco/11/GRCh38#36464000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101546303-C-A

36464000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546303-C-G

36464000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546303-C-T

36464007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546295-A-G

36464059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546231-A-T

36464107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546175-G-A

36464107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546175-G-T

http://identifiers.org/hco/11/GRCh38#36464112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101546170-C-A

36464112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546170-C-T

http://identifiers.org/hco/11/GRCh38#36464114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101546168-C-A

36464114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546168-C-T

http://identifiers.org/hco/11/GRCh38#36464202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101546076-C-A

36464239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101546000-G-C

http://identifiers.org/hco/11/GRCh38#36464258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101545955-C-A

http://identifiers.org/hco/11/GRCh38#36464471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101545613-A-C

36464564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101545490-A-G

36464806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 101545018-G-T

36465057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3 prime UTR variant
orthologous variants: 101544768-G-T

36465062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3 prime UTR variant
orthologous variants: 101544763-A-G

36465075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25878
most severe consequence: 3 prime UTR variant
orthologous variants: 101544750-A-G