119334902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 5 prime UTR variant
orthologous variants: 116426890-G-T

http://identifiers.org/hco/12/GRCh38#119335034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116426784-A-C

119335087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116426731-A-G

119335129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116426688-A-G

119335247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116426523-C-T

119335274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116426496-T-A

119340957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116423640-A-G

http://identifiers.org/hco/12/GRCh38#119341151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116423208-C-A

119341218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116423143-A-G

119341219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116423142-A-G

http://identifiers.org/hco/12/GRCh38#119341315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116423053-C-A

119341340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116423032-G-T

119341360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116423009-G-C

119341360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116423009-G-T

119341365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116423004-G-T

119341377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422992-G-T

119341883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422368-C-G

119342012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422239-T-G

119342046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422205-A-G

119342143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422122-G-T

119342263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116422047-T-A

119342342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116421972-T-A

http://identifiers.org/hco/12/GRCh38#119342997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116420674-C-A

119343195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116420470-C-G

119343195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116420470-C-T

119343301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116420367-C-T

119343558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116420149-C-T

119343614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116420091-A-G

119346584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116416876-G-A

119346676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116416780-T-C

119347374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116416460-T-A

http://identifiers.org/hco/12/GRCh38#119347747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116415363-A-C

119347802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116415307-C-G

http://identifiers.org/hco/12/GRCh38#119347845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116415261-C-A

119348089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116414998-T-C

119348170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116414919-G-T

119348218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116414886-T-G

119353219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116413239-T-C

119353219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116413239-T-G

119353227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116413231-G-A

119354081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116412953-C-G

119354119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116412913-T-C

119354138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116412894-C-T

http://identifiers.org/hco/12/GRCh38#119354185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116412846-C-A

119354185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116412846-C-T

119354309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116412718-A-G

119354553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116412528-T-G

http://identifiers.org/hco/12/GRCh38#119354698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116412378-C-A

http://identifiers.org/hco/12/GRCh38#119364295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116410249-C-A

119364403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116410174-A-T

119364778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116409811-C-T

119364792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116409797-G-C

119364858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116409732-G-A

119364925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116409665-G-A

119364969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116409620-A-G

http://identifiers.org/hco/12/GRCh38#119364999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116409590-A-C

119365015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116409574-G-A

119365015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116409574-G-C

http://identifiers.org/hco/12/GRCh38#119365077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116409512-C-A

119365077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116409512-C-G

119368523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116408233-G-A

119368523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116408233-G-T

119368642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116408125-A-G

119368765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116407988-C-T

119368963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116407820-A-T

119368981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116407802-G-A

119369294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116407524-C-T

119369375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116407454-G-A

119369851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116406732-G-A

119370004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116406593-T-C

119370004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116406593-T-G

119370072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116406542-G-A

119370097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116406521-G-A

http://identifiers.org/hco/12/GRCh38#119370107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116406511-A-C

119370286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116406329-G-A

119370313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116406319-C-T

119370493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116406140-T-C

119370576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116406082-G-T

119370577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116406081-G-T

119371099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

119371168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

119371175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

119371225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

119371252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

119371364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

119371377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

119371517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

119373837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116404668-C-T

119373859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116404646-G-T

119374006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116404510-C-T

119374392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116404224-T-A

119374396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116404220-C-T

119378641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403447-G-T

119378671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403417-C-T

119378674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403414-C-T

119378777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403317-A-G

119378900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403201-C-T

119378963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403142-C-T

119378999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403106-C-T

119379100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116403009-G-A

119379408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402697-C-T

119379686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402436-A-G

119379744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402385-G-T

119379746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402383-G-A

119379803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402330-A-G

119379833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402295-C-G

119379837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402291-A-T

http://identifiers.org/hco/12/GRCh38#119379852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116402274-A-C

119379996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402245-G-A

119380010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402231-A-G

119380069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402172-G-A

119380172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402063-T-C

119380172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116402063-T-G

http://identifiers.org/hco/12/GRCh38#119380348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116401914-C-A

119380348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116401914-C-T

119380430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116401634-G-C

http://identifiers.org/hco/12/GRCh38#119380464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116401600-C-A

119380464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116401600-C-T

119380490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116401588-G-A

http://identifiers.org/hco/12/GRCh38#119380864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116401234-C-A

119380993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400603-G-A

119381051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400545-A-G

http://identifiers.org/hco/12/GRCh38#119381130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116400478-A-C

119381160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400448-G-C

http://identifiers.org/hco/12/GRCh38#119381192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116400417-A-C

http://identifiers.org/hco/12/GRCh38#119381258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116400351-A-C

119381292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400336-C-T

119381400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400233-G-T

119381435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400198-T-C

119381606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400026-G-C

119381614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116400018-C-T

119383421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399348-C-T

119383537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399228-C-T

119383602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399158-C-T

http://identifiers.org/hco/12/GRCh38#119383720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116399099-C-A

119383823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116399010-G-A

119384265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116398888-G-T

119384314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116398854-G-C

119384350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116398827-T-C

http://identifiers.org/hco/12/GRCh38#119384524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116398653-C-A

119384560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116398617-G-A

119384683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116398525-G-A

119386086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116397234-T-C

119386094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116397226-A-G

119386496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116396873-T-A

119386496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116396873-T-C

119386636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116396757-C-T

http://identifiers.org/hco/12/GRCh38#119386718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116396675-C-A

119386718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116396675-C-T

119386992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116396418-C-G

119386992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116396418-C-T

119387023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116396387-C-G

119387023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116396387-C-T

119388889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116393804-C-G

119388909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116393784-T-G

119388988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116393706-C-T

119388989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116393705-C-T

119389034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116393648-T-A

119389149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116393498-T-G

119389203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116393452-T-C

119389205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116393450-G-T

119389261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116393396-C-T

119390823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116392063-G-A

119391106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391789-A-G

119391149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391753-G-A

119391149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391753-G-C

119391297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391522-A-G

119391387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391432-A-G

119391399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391420-C-G

119391412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391407-G-A

119391511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116391308-C-T

119391696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116390986-T-C

119391753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116390016-T-C

119392016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116389698-A-G

119392095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116389633-A-G

119392119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116389613-G-T

119393244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116385378-A-G

119393298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116385317-A-G

119393420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116385198-C-T

http://identifiers.org/hco/12/GRCh38#119393624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116385056-A-C

119393982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116384600-C-T

119394105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116384469-C-T

119394585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116383444-A-T

119394845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116383157-T-C

119394967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116383056-T-A

119394989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116383034-G-T

119395008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116383015-G-C

119395114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382890-A-G

119395197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382818-G-A

119399717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116381020-C-T

http://identifiers.org/hco/12/GRCh38#119399740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116380997-A-C

119399740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116380997-A-G

119399776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116380948-C-T

119401526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379799-T-C

119401722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379642-T-C

119401739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379625-C-G

119401844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379520-T-C

119401900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379456-T-C

119401949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379407-T-C

119404572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377536-T-G

119404766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377355-G-T

119404979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377178-T-C

119404979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377178-T-G

119404984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377160-C-T

http://identifiers.org/hco/12/GRCh38#119404985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116377159-C-A

119405142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377052-C-T

119405194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116376999-G-A

http://identifiers.org/hco/12/GRCh38#119405215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116376978-C-A

119405239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116376953-C-T

119405245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116376947-G-C

119405499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116376690-G-A

119405499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116376690-G-C

119405513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116376676-T-C

119406204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116375340-T-G

119406345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116375198-T-C

119406557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116374980-T-C

119406700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116374854-G-A

119406818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116374750-G-A

119406827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116374741-G-A

119408115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116373380-G-T

119408129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116373366-G-A

119408190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116373305-T-G

119408208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116373288-G-T

119410191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116372239-G-C

119410191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116372239-G-T

119410264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116372175-A-G

119410521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116371911-T-C

119410545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116371887-C-T

119410633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116371819-G-C

119412143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116370938-T-C

http://identifiers.org/hco/12/GRCh38#119412862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116370466-C-A

119412862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116370466-C-T

119412980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116370389-A-G

119413132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116370265-G-A

119413224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116370157-A-G

119413459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116369935-C-T

119413566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116369840-G-A

119413655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116369757-G-A

119421033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116368496-G-A

119421041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116368488-T-C

119421519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116367944-C-T

119421559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116367906-A-G

119421766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116367737-G-T

119422025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116367646-G-A

119422130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116367599-A-G

119422172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116367586-C-T

119423283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116366931-A-G

119423308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116366910-A-G

119423528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116366682-A-G

http://identifiers.org/hco/12/GRCh38#119423726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116366519-A-C

119423726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116366519-A-G

119424443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116365874-A-G

http://identifiers.org/hco/12/GRCh38#119428613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116363479-C-A

119428613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116363479-C-T

119436940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116358618-A-G

119437035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116358520-A-G

119437081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116358484-G-A

119438186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116357348-T-A

119438454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116357086-G-C

119438588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116356986-G-C

119438766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116356818-A-G

119438909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116356684-C-T

119439017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116356592-A-G

119439272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116356293-T-G

119439277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116356288-G-A

119439326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116356253-G-A

119439653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116355757-G-C

119439697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116355713-G-C

119439755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116355655-A-T

119444049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116351111-G-A

119444809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116350800-C-T

119444831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116350778-T-C

119444937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116350714-T-C

119446147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116350180-T-C

http://identifiers.org/hco/12/GRCh38#119446170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116350157-A-C

http://identifiers.org/hco/12/GRCh38#119446173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116350151-A-C

http://identifiers.org/hco/12/GRCh38#119446214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116350109-C-A

http://identifiers.org/hco/12/GRCh38#119446902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116348705-A-C

119447139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116348475-T-G

119447676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116347961-A-G

http://identifiers.org/hco/12/GRCh38#119447688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116347949-C-A

119447704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116347946-C-T

http://identifiers.org/hco/12/GRCh38#119447715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116347935-C-A

119447754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116347896-G-T

119447798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116347856-T-A

119447798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116347856-T-C

119447832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116347850-G-A

119447838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116347844-G-A

119447838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116347844-G-T

119448159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116347626-T-A

119448289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116347497-T-C

119448313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116347415-G-T

119448556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116347209-A-G

119448659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116347086-G-C

119448986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116346749-G-A

119449225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116346466-C-G

119449332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116345894-T-C

119449396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116345823-G-A

119449469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116345665-A-G

119449469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116345665-A-T

119449611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116345549-A-G

http://identifiers.org/hco/12/GRCh38#119452014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116343321-C-A

119452014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116343321-C-T

119452091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116343247-T-A

119452351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116342983-T-C

119452353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116342981-T-C

119452708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116342661-G-T

119452734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116342635-G-A

119452757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116342615-G-C

119453255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116341401-T-C

119453407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116341262-G-A

http://identifiers.org/hco/12/GRCh38#119453456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116341213-C-A

119457504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116336606-G-C

119457653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116336459-T-C

119457803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116336313-C-G

119457892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116336224-A-G

119457957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116336157-T-C

119457964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116336150-T-C

119457967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116336147-T-C

119457981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116336130-G-A

119458295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116335841-C-T

http://identifiers.org/hco/12/GRCh38#119458296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116335840-A-C

119458321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116335815-G-A

119458443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116335700-T-C

119458447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116335696-A-T

119458513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116335634-T-C

119458520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116335629-G-A

119458613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116335521-T-A

119460338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116334172-A-G

119460479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116334051-T-A

119460509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116334022-A-G

119461910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116331812-G-A

119461945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116331778-T-C

http://identifiers.org/hco/12/GRCh38#119462001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116331724-A-C

119462001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116331724-A-T

119462021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116331705-C-G

119470224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116331337-A-G

119470345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116331187-T-G

119470476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116331071-A-G

119470724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116330478-T-A

119470791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116330405-C-T

119470837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116330360-C-T

119471146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116330059-G-A

119471189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116330028-A-G

119471247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329974-G-C

119471263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329958-T-A

119471263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329958-T-C

119471417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329805-C-G

http://identifiers.org/hco/12/GRCh38#119471421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116329801-C-A

119471878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116328379-C-G

119471878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116328379-C-T

119471948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116328311-T-C

119472136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116328145-G-C

119472187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116328108-G-A

119472347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116327964-T-G

119472350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116327961-A-G

119472521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116327652-C-T

http://identifiers.org/hco/12/GRCh38#119474442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116326572-C-A

119475367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116322423-T-A

http://identifiers.org/hco/12/GRCh38#119475620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116322186-C-A

http://identifiers.org/hco/12/GRCh38#119475739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116322073-A-C

119475940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116321877-A-G

119475940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116321877-A-T

119476184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116321385-C-T

119476265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116321276-C-T

119476889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116320687-T-A

119477498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116320153-G-A

119477734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116319949-A-G

119477903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116319745-C-T

119477905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116319743-C-T

119477906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116319742-A-G

http://identifiers.org/hco/12/GRCh38#119477907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116319741-C-A

119477908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116319740-A-G

119477912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116319736-A-G

119477923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116319725-C-G

119478919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116319141-T-A

119478962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116319094-C-T

119479018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116319043-G-T

http://identifiers.org/hco/12/GRCh38#119479065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116318998-C-A

119479146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116318916-C-T

http://identifiers.org/hco/12/GRCh38#119479222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116318839-C-A

119479223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116318838-T-A

119479223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116318838-T-G

119479296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116318771-C-T

119479368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116318691-T-C

http://identifiers.org/hco/12/GRCh38#119479429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116318617-C-A

119479429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116318617-C-T

119479469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116318581-G-T

http://identifiers.org/hco/12/GRCh38#119479489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116318561-C-A

119479489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 116318561-C-T

119479490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116318560-T-C

119479539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116318487-T-C

http://identifiers.org/hco/12/GRCh38#119479548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116318478-C-A

119479548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116318478-C-T

119479573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116318455-C-T

119479651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116318374-C-T

119479696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116318328-T-A

119479752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116318290-G-T

119479753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116318289-A-G

119479760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116318282-G-T

119479774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116318273-G-C

http://identifiers.org/hco/12/GRCh38#119479811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116318252-C-A

119479811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116318252-C-T

119479873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116318199-G-T

119481186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116317997-T-C

119481224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116317945-G-A

http://identifiers.org/hco/12/GRCh38#119481330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116317823-C-A

119481331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116317822-A-G

http://identifiers.org/hco/12/GRCh38#119481350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116317802-C-A

119481350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116317802-C-G

119483324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116315316-C-T

119483452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116315181-C-G

119483667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116315018-T-C

119483769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116314958-G-A

119483821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116314906-T-C

119483915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116314835-C-T

119483967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116314751-A-T

119484088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116314621-C-T

119484817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116314263-A-G

119485722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116313874-A-G

119485735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116313861-G-T

119485736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116313860-T-G

119485748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116313855-G-A

119485817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116313786-G-A

119485871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116313726-T-A

119486009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116313515-T-C

119486125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116313430-T-A

119486634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116313220-G-A

119486638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116313216-G-A

119486686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116313178-C-T

119487002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116312901-T-C

119487183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116312738-C-T

http://identifiers.org/hco/12/GRCh38#119488632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116310690-C-A

119488632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116310690-C-T

119488729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116310636-C-T

119488745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116310620-C-G

119488920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116310436-G-A

119488952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116310406-T-G

119488999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116310363-T-C

119489013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116310350-A-G

119489014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116310349-G-A

119489014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116310349-G-T

119489061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116310320-T-G

119489212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116310179-A-T

119490871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116309103-T-G

119491071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308896-C-T

119491608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308726-A-G

119491636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308701-A-G

119491639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308698-T-C

119491726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308597-T-A

119491726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308597-T-C

119491728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308595-C-T

119491897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308425-A-G

119491923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308399-G-A

119491923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308399-G-C

119492006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308317-G-C

119492090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308235-C-T

119492217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308123-A-G

119492217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116308123-A-T

119495589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116306128-C-T

119495950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116305594-C-T

119496007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116305511-G-A

119496164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116305359-C-T

119496197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116305312-A-G

119496220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116305289-C-G

119496652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116304896-C-G

119497155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116304316-G-T

119497181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116304290-T-G

119497269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116304211-C-T

119497443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116304035-G-A

119497821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116303678-A-G

119497821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116303678-A-T

119498059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116303449-G-C

119498258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116303284-A-T

119498884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116302747-C-T

http://identifiers.org/hco/12/GRCh38#119499101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116302527-C-A

119499101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116302527-C-T

119499407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116302274-G-A

119499534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116302193-C-T

119499855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116301872-T-C

119499859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116301865-C-T

119499956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116301768-G-A

119499956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116301768-G-T

119500157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116301551-A-G

119500166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116301542-A-G

http://identifiers.org/hco/12/GRCh38#119500174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116301534-C-A

119500529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116298972-C-G

119500529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116298972-C-T

119501089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116298744-G-A

119501196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116298638-T-C

119501331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116298380-A-T

119501379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116298336-T-C

119501454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116298274-G-A

http://identifiers.org/hco/12/GRCh38#119501605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116298157-C-A

119501737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116298040-A-G

119501767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116298029-G-C

119501962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297839-G-A

119502117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297646-T-A

119502117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297646-T-C

119502230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297560-C-T

119502405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297372-T-C

119502545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297211-T-C

119502568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116297188-C-T

119502881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116296896-T-G

119504934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116295920-A-G

119505035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116295811-T-G

119505201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116295622-T-C

119505233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 116295611-G-A

http://identifiers.org/hco/12/GRCh38#119505379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116295474-C-A

119505379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116295474-C-T

119505384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116295468-G-T

119505423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116295393-A-G

http://identifiers.org/hco/12/GRCh38#119505445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116295371-C-A

119505445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116295371-C-T

119512975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116293155-T-C

119512980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116293150-G-T

119516468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284402-T-C

http://identifiers.org/hco/12/GRCh38#119516502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116284368-C-A

119516502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284368-C-T

119516528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284342-G-T

119516533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284337-G-T

http://identifiers.org/hco/12/GRCh38#119516565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116284310-C-A

119516565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284310-C-T

119516597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284289-A-G

119516603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284283-A-G

119516603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284283-A-T

119516712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284174-G-A

119516712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284174-G-T

http://identifiers.org/hco/12/GRCh38#119516717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116284169-C-A

http://identifiers.org/hco/12/GRCh38#119516766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116284117-A-C

119516808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284088-A-T

119516832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284061-T-C

http://identifiers.org/hco/12/GRCh38#119516833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116284060-C-A

119516833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284060-C-T

http://identifiers.org/hco/12/GRCh38#119516834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116284059-A-C

119516834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284059-A-G

http://identifiers.org/hco/12/GRCh38#119516852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116284041-A-C

119516852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116284041-A-G

119517607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116282473-A-G

119517712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116282364-T-C

119517713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116282363-C-G

119517836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116282232-G-A

119517963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116282100-A-G

http://identifiers.org/hco/12/GRCh38#119518131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116281937-C-A

119518133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116281935-G-A

119518133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116281935-G-T

119518148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116281920-A-G

http://identifiers.org/hco/12/GRCh38#119518213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116281864-A-C

119519872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116279196-G-A

http://identifiers.org/hco/12/GRCh38#119520012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116279010-C-A

http://identifiers.org/hco/12/GRCh38#119520041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116278979-C-A

119520206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116278822-G-A

119520230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116278757-G-A

119520231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116278756-G-A

119520375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116278586-A-G

119522083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116276409-G-A

119522223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116276154-G-A

119522223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116276154-G-C

119522765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275328-G-A

119522793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275300-T-A

119522793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275300-T-C

119522798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275295-G-A

119522798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275295-G-C

119522798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275295-G-T

http://identifiers.org/hco/12/GRCh38#119522833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116275252-C-A

119522833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275252-C-T

http://identifiers.org/hco/12/GRCh38#119522840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116275245-C-A

119522840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275245-C-G

119522854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275225-C-G

119522854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275225-C-T

119522875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275204-T-C

119522876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275203-G-A

119522994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116275096-T-C

119523006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275084-G-T

http://identifiers.org/hco/12/GRCh38#119523067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116275016-C-A

119523076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275007-G-A

119523076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275007-G-T

119523078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116275005-A-G

119523095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274988-G-C

119523103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274980-T-A

119523103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274980-T-C

119523103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274980-T-G

http://identifiers.org/hco/12/GRCh38#119523246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116274858-A-C

119523279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274828-G-A

119523325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274790-C-T

119523484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274683-G-A

119523536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274650-C-T

119523541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274645-G-A

119523541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274645-G-T

119523584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274610-G-T

119523593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274601-G-T

119523610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274584-T-G

119523617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274577-G-A

119523617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274577-G-C

119523646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274548-A-G

119523660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274534-C-T

119523696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 116274506-C-T

http://identifiers.org/hco/12/GRCh38#119523700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116274502-A-C

119523827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274378-A-G

119523883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274321-A-G

119523973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274233-A-G

119524132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116274092-T-A

119524261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116273959-T-A

119524261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116273959-T-C

119528371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116272501-G-A

119528371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116272501-G-T

119528385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116272489-G-A

http://identifiers.org/hco/12/GRCh38#119528468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116272393-C-A

http://identifiers.org/hco/12/GRCh38#119528495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116272348-C-A

119528495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116272348-C-T

http://identifiers.org/hco/12/GRCh38#119528536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116272308-C-A

119528560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116272284-G-A

119528560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116272284-G-T

119528561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116272283-G-A

119528561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116272283-G-C

119528562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116272282-T-C

http://identifiers.org/hco/12/GRCh38#119528600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116272231-C-A

119528758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116272074-A-G

http://identifiers.org/hco/12/GRCh38#119528854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116271999-C-A

119528854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116271999-C-T

119528878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116271952-A-T

http://identifiers.org/hco/12/GRCh38#119528891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116271939-C-A

119528891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116271939-C-G

119528891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116271939-C-T

119529246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116271134-A-T

119529534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270836-A-G

119529538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270832-T-C

119529654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270715-G-C

http://identifiers.org/hco/12/GRCh38#119529694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116270675-A-C

119529695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270674-C-G

119529695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270674-C-T

119529782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270556-G-A

119529782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270556-G-C

119529782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270556-G-T

119529919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270459-C-T

119529955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270416-A-G

http://identifiers.org/hco/12/GRCh38#119529962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116270409-C-A

119529962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270409-C-T

http://identifiers.org/hco/12/GRCh38#119530157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116270224-A-C

119530157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270224-A-G

119530207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270183-T-C

119530249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270089-A-G

119530259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116270079-G-T

http://identifiers.org/hco/12/GRCh38#119530768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116269402-C-A

119530768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116269402-C-T

http://identifiers.org/hco/12/GRCh38#119530779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116269391-C-A

119530989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116269155-C-T

119531049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116269095-G-A

119531049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116269095-G-T

119531145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116269036-G-A

http://identifiers.org/hco/12/GRCh38#119531205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116268960-C-A

119531205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116268960-C-T

119531211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116268954-A-T

119531346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116268820-C-G

119531433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116268738-T-G

119531980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116267115-A-G

119531980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116267115-A-T

119532152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116266965-C-T

119540309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116266354-T-C

119540589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116264259-G-A

119540589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116264259-G-T

119540632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116264216-A-G

119540663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 116264185-G-A

119540794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116264066-G-T

119541001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116263884-T-C

http://identifiers.org/hco/12/GRCh38#119541004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116263881-A-C

119541004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116263881-A-G

119541004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116263881-A-T

http://identifiers.org/hco/12/GRCh38#119541005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116263880-C-A

http://identifiers.org/hco/12/GRCh38#119541010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116263875-C-A

119541010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28610
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116263875-C-T