91160638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36323645-G-T

91160645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36323652-A-G

91160907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36323884-G-C

91161151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36324104-G-A

91161380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5 prime UTR variant
orthologous variants: 36324323-A-G

91161485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5 prime UTR variant
orthologous variants: 36324444-G-A

91161485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5 prime UTR variant
orthologous variants: 36324444-G-T

91162215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5 prime UTR variant
orthologous variants: 36325082-T-C

91162224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5 prime UTR variant
orthologous variants: 36325091-G-A

91162260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5 prime UTR variant
orthologous variants: 36325117-A-T

91162278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5 prime UTR variant
orthologous variants: 36325135-G-A

91162316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5 prime UTR variant
orthologous variants: 36325172-T-A

91162316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5 prime UTR variant
orthologous variants: 36325172-T-C

91162316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5 prime UTR variant
orthologous variants: 36325172-T-G

91162628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36325484-G-A

91162635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36325490-G-A

91162702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36325556-G-A

91162702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36325556-G-C

91162966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36325851-G-A

91163488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36326332-G-T

91163548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36326391-C-T

91163888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36326654-C-T

91163969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36326709-G-C

91164338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36327014-G-A

91164513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36327194-C-G

http://identifiers.org/hco/10/GRCh38#91164824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36327515-C-A

http://identifiers.org/hco/10/GRCh38#91164898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36327588-C-A

91164900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36327590-G-T

91165121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36327811-C-T

91165157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36327850-T-C

91165157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36327850-T-G

91165414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328085-A-G

91165596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328155-A-G

91165602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328159-A-G

91165891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328431-G-A

91165891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328431-G-T

91165898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328438-T-A

91165963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328495-A-G

91165993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328523-A-G

91166177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328686-T-C

91166205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328716-C-G

91166240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328751-C-T

91166271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328782-A-G

91166369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36328880-T-C

91166579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36329038-A-G

91166787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36329254-A-G

91167015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36329604-C-G

91167015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36329604-C-T

91167016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36329605-G-A

91167091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36329690-T-C

91167556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36330112-A-T

91167701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36330252-A-G

91169847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36331912-A-G

91169866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36331921-A-G

91170181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36332183-A-G

91170239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36332239-A-G

91170239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36332239-A-T

91170729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36332709-T-C

91170732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36332716-T-C

91170736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36332720-C-T

91170820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36332819-A-G

http://identifiers.org/hco/10/GRCh38#91170836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36332835-A-C

91170836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36332835-A-G

91170977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36333076-A-G

91171040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36333183-C-G

91171370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36333633-A-G

91171396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36333655-G-A

91171471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36333729-T-C

91171570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36333827-A-G

91171772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36334008-C-T

91171804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36334031-A-G

91171848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36334076-C-T

91172350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36334576-C-T

http://identifiers.org/hco/10/GRCh38#91172695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36334993-C-A

91172698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36334996-C-G

91172765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36335048-A-T

91173021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36335422-C-T

91173053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36335455-G-A

91173097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36335498-T-C

91173248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36335649-G-A

91173324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36335709-C-T

http://identifiers.org/hco/10/GRCh38#91173626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36335994-C-A

91173626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36335994-C-T

91173809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36336190-A-G

91174198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36336438-T-G

91186954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36342028-A-G

91187077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36342130-C-G

91187374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36342435-C-T

91187392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36342451-T-C

91187448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36342494-C-G

91187838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36342825-A-G

91188772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36343541-T-A

91188796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36343564-G-A

91188796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36343564-G-C

91189048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36343723-A-G

91189076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36343751-A-G

91189112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36343795-A-G

91189297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36343954-T-C

91189337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36343993-A-G

91189607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36344286-A-G

91189608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36344287-T-C

91189670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36344346-T-C

91189857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36344700-A-G

91189864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36344707-T-C

91190007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36344846-G-T

91190066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36344906-T-A

91190066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36344906-T-C

91190298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36345126-G-A

91190298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36345126-G-T

91190315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36345143-T-C

91190468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36345250-C-G

91190468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36345250-C-T

91190697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36345487-G-A

91190817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36345616-A-G

91191666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36345896-A-G

91191666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36345896-A-T

91191670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36345900-C-T

91191778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36346012-G-A

91191849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36346084-G-A

http://identifiers.org/hco/10/GRCh38#91191992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36346391-C-A

91192249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36346638-G-A

91192286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36346679-A-G

91192287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36346680-C-T

91192429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36346939-A-G

http://identifiers.org/hco/10/GRCh38#91192569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36347097-C-A

91192667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36347182-C-T

91192806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36347302-A-G

91193118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36347451-G-A

http://identifiers.org/hco/10/GRCh38#91193131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36347464-C-A

91193131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36347464-C-T

91193229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36347538-G-A

91193431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36347709-A-G

91193677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36347919-T-C

91193754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36347998-G-T

91194656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36348904-T-C

91196402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36349748-C-T

91196409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36349756-C-G

91196486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36349836-T-C

91196503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36349852-C-T

91196530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36349877-G-A

91196551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36349898-G-A

91196622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36349964-T-C

91197117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36350296-C-T

91197212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36350382-C-T

91197233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36350403-G-T

91197247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36350420-G-A

91197254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36350427-T-A

http://identifiers.org/hco/10/GRCh38#91197279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36350444-A-C

91197378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36350545-G-A

91197378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36350545-G-T

91197490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36350657-G-A

91198787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36352808-A-G

91198811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36352832-T-C

91198948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36352951-T-G

91199022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36353028-T-G

91199163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36353182-A-G

91199205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36353221-A-G

91199664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36354196-G-T

91200133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36355003-C-T

91200219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36355062-A-G

91200320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36355149-C-G

91200437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36355321-G-A

91200488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36355389-T-C

91200503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36355421-A-G

91200570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36355500-C-T

91200716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36355632-A-G

91200853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36355773-G-A

91200913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36355820-G-A

91201012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36355920-T-C

http://identifiers.org/hco/10/GRCh38#91201533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36356022-C-A

91201533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36356022-C-T

91201679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36356186-G-T

http://identifiers.org/hco/10/GRCh38#91201709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36356216-A-C

91201746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36356257-C-T

91201873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36356371-T-G

91201944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36356441-G-C

91202006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36356499-C-T

91202196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36356683-G-A

91202221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36356732-A-G

91202469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36356948-G-A

91202506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36356987-T-G

91202645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36357132-C-T

91202735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36357209-G-A

91202801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36357280-G-C

91202870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36357340-A-G

http://identifiers.org/hco/10/GRCh38#91202872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36357342-A-C

91202944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36357412-T-G

http://identifiers.org/hco/10/GRCh38#91203077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36357649-A-C

91203146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36357808-T-C

91203158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36357820-G-T

91203272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36357964-A-G

91203272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36357964-A-T

91204682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360366-C-T

91204686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360370-A-G

91204753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360454-T-G

91204921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360628-A-G

91204962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360672-A-G

91205216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360906-G-A

91205249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360916-T-C

91205323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360989-A-G

91205353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361018-G-T

http://identifiers.org/hco/10/GRCh38#91205366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36361031-A-C

91205380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361045-A-G

91205598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361252-A-G

91205598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361252-A-T

91206050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361375-G-A

91206050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361375-G-C

91206125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361447-G-C

91206202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361518-T-C

91206202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361518-T-G

91206251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361565-G-A

91206422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361744-T-C

91206465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361781-C-T

http://identifiers.org/hco/10/GRCh38#91206535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36361848-A-C

91206710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361998-G-C

91206788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362070-G-T

91206829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362116-A-G

91206886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362308-T-C

91206951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362382-A-G

91207012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362442-C-G

91207020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362445-A-G

91207166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362545-T-G

91207180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362559-A-G

91207374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362756-G-A

91208720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36364448-C-G

91208785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36364509-C-T

91208794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36364518-G-A

91208798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36364522-C-T

91208819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36364543-A-G

91209865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365433-A-G

91209865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365433-A-T

91210237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365730-C-T

91210253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365743-C-T

91210297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365795-G-A

http://identifiers.org/hco/10/GRCh38#91210432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36365899-C-A

91210571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36366036-G-A

91211217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36366700-A-G

http://identifiers.org/hco/10/GRCh38#91211541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36367019-C-A

91211699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36367156-G-C

91212006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36367352-A-T

91212326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36367670-T-C

91212717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36368036-T-C

91213408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36374156-A-G

http://identifiers.org/hco/10/GRCh38#91214994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36375310-A-C

91215221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36375550-G-A

91215710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36379798-C-T

91215722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36379827-A-G

91215774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36379882-T-C

91215933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36380438-T-G

91216085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36380576-C-T

91216422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36381197-G-T

91216623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36381444-T-C

http://identifiers.org/hco/10/GRCh38#91216698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36381507-A-C

91216998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36381808-A-G

91219689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36385731-G-T

91219756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36385806-A-G

91219830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36385875-G-A

91220046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36386300-G-T

91220110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36386365-A-G

http://identifiers.org/hco/10/GRCh38#91220122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#36386377-C-A

http://identifiers.org/hco/10/GRCh38#91220203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#36386420-C-A

91220274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36386492-G-A

91220275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36386493-G-A

91220275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36386493-G-T

http://identifiers.org/hco/10/GRCh38#91220438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36386855-C-A

http://identifiers.org/hco/10/GRCh38#91220503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#36386943-C-A

91220503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36386943-C-T

91220559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36387017-G-T

91220807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36387285-G-A

91220807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36387285-G-C

91220807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36387285-G-T

91220904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36387359-G-A

91221171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36387572-C-G

91221173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36387574-G-C

91221512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36387855-C-T

91221520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36387863-G-A

91221708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36388091-T-A

http://identifiers.org/hco/10/GRCh38#91221740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36388125-C-A

91221818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36388292-A-T

91221832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36388306-G-A

91222120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36388828-G-A

91222214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36388929-G-A

91222424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36389118-A-G

http://identifiers.org/hco/10/GRCh38#91222576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36389272-C-A

91222576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36389272-C-T

91222643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36389323-T-C

http://identifiers.org/hco/10/GRCh38#91222657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36389336-C-A

91222657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36389336-C-T

http://identifiers.org/hco/10/GRCh38#91222706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36389372-C-A

http://identifiers.org/hco/10/GRCh38#91222790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36389451-C-A

91222790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36389451-C-T

http://identifiers.org/hco/10/GRCh38#91223009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36389662-C-A

91223009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36389662-C-T

91223026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36389686-G-A

91223053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36389720-T-G

91223138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36389799-T-C

91223380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36390143-A-G

91223547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36390292-T-C

91223620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36390360-C-T

91223641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36390378-T-C

91223890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36390623-G-A

91223949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36390672-T-A

91223949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36390672-T-C

91224142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36390826-T-C

91224690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36391283-G-A

91224843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36391438-T-C

91224879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36391481-A-G

91224879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36391481-A-T

91224897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36391510-G-A

91224957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36391568-C-T

91225404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36393610-C-T

91225419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36393625-A-G

91225428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36393634-A-T

91225466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36393668-T-C

91225578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36393751-G-A

91225815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36393884-G-A

http://identifiers.org/hco/10/GRCh38#91225964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36394038-C-A

91226072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394158-A-G

http://identifiers.org/hco/10/GRCh38#91226101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36394179-A-C

91226315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394397-T-A

91226315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394397-T-G

91227519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395631-T-C

91227519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395631-T-G

http://identifiers.org/hco/10/GRCh38#91227521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36395633-C-A

91227521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395633-C-G

http://identifiers.org/hco/10/GRCh38#91227532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36395644-C-A

91227542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395654-T-C

http://identifiers.org/hco/10/GRCh38#91227546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36395658-C-A

91227623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395725-G-T

91227625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395727-G-A

91227625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395727-G-T

91227669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395778-T-A

http://identifiers.org/hco/10/GRCh38#91227671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36395780-A-C

91227674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395783-C-T

91227679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395793-T-C

91227680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395794-A-T

91227783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395888-C-T

http://identifiers.org/hco/10/GRCh38#91227810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36395915-C-A

91227810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36395915-C-T

91227892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36396008-A-G

91227936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36396061-G-A

91227936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36396061-G-C

91227960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36396085-A-G

91227960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36396085-A-T

91228071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36396209-T-C

91228466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36396794-T-G

http://identifiers.org/hco/10/GRCh38#91228629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36397163-A-C

91229055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36397663-A-T

91229204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36397808-G-A

91229215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36397819-A-G

91229922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36398523-T-C

91229923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36398524-A-G

91230124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36398717-A-G

91230264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36398855-G-A

91230429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36399009-G-A

91232003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36404318-A-G

91232060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36404384-G-A

91232223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36404509-G-A

91232303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36404584-T-C

91232476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36404811-G-A

91232476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36404811-G-C

91232657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36404949-A-G

91232811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36405075-G-C

91233560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36405986-C-T

91233592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36406002-A-G

91233616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36406018-G-A

91233737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36406126-G-A

91233925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36406529-A-G

91233983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36406580-A-G

91234571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36407095-G-A

91234590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36407107-T-G

91234783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36407275-G-A

91234942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36407421-T-A

91234996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36407475-A-G

91235051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36407529-A-G

91235128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36407614-G-A

91235308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36407766-G-A

91236848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36408185-A-G

91237029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36408383-A-G

91237053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36408413-A-G

91237140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36408488-A-G

91237183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36408529-A-T

91237628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36409176-C-T

91237681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36409212-T-G

91237688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36409219-G-A

91237690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36409221-G-C

91238070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36409674-A-G

91238223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36409823-T-C

91238239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36409839-A-G

91238325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36409924-A-G

91238368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36409967-A-T

91238490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36410090-G-T

91238533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36410120-G-C

91238846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36410424-C-T

91238867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36410457-T-G

91239138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36410754-G-A

91239335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36410934-A-G

http://identifiers.org/hco/10/GRCh38#91239598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36411196-A-C

91239718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36411309-G-A

91240101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36411721-A-G

91240178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36411800-C-T

91240249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36411853-T-G

91240280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36411884-T-G

91240300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36411905-G-A

91240420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36411942-T-C

91240420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36411942-T-G

91240665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36412143-G-A

91240665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36412143-G-C

91240665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36412143-G-T

http://identifiers.org/hco/10/GRCh38#91240670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36412148-C-A

91240670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36412148-C-T

91240726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36412200-G-T

91246658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36412454-A-G

http://identifiers.org/hco/10/GRCh38#91247586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36413579-C-A

91247882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36413845-T-C

91247919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36413882-T-C

91248251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36414141-G-A

91248492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36414545-C-T

91248801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36414819-G-A

91249185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36415156-A-G

91249218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36415186-T-A

91251080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36417201-A-T

http://identifiers.org/hco/10/GRCh38#91251434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36417541-A-C

91251779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36417995-G-A

91251967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36418191-T-C

91252102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36418298-T-A

91252102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36418298-T-C

91252221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36418413-C-G

91252491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36418675-T-C

91252502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36418686-A-G

91252506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36418690-A-G

91259301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36419652-C-T

http://identifiers.org/hco/10/GRCh38#91261178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36419956-C-A

91261178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36419956-C-T

91261252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36420029-A-G

91261274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36420188-A-G

http://identifiers.org/hco/10/GRCh38#91262883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36421101-C-A

91263112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36421279-G-A

91263112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36421279-G-T

91263254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36421408-T-C

91263349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36421501-G-A

91263349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36421501-G-T

91263456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36421590-T-C

http://identifiers.org/hco/10/GRCh38#91263465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36421606-C-A

91263547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36421683-A-G

91263809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36421910-G-T

91263857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36421957-A-G

91263957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36421973-C-T

91264022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36422039-T-C

91264178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36422166-T-C

91264223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36422211-A-G

91264246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36422232-A-G

91264257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36422251-A-G

91264257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36422251-A-T

91264371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36422327-A-G

http://identifiers.org/hco/10/GRCh38#91264398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36422357-A-C

91264398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36422357-A-G

91265067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36422944-A-G

91265695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36423437-A-G

91265911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36423709-G-T

91266341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36424238-G-A

91266341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36424238-G-C

91266364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36424293-G-A

91268248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36424925-A-G

91268434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36425084-G-A

91268509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36425148-A-G

91268717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36425357-A-G

http://identifiers.org/hco/10/GRCh38#91268807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36425459-C-A

91268807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36425459-C-G

91268833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36425484-T-G

91268847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36425498-A-T

91268923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36425573-G-T

91269085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36425729-G-A

http://identifiers.org/hco/10/GRCh38#91269665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36426247-A-C

91269711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36426279-A-G

91269736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36426298-C-G

91269736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36426298-C-T

91269904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36426441-G-A

91269904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36426441-G-C

91269924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36426463-C-G

91270463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36426972-C-T

91271078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36427386-T-C

91271293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36427602-G-C

http://identifiers.org/hco/10/GRCh38#91271432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36427777-C-A

91271844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36428313-G-T

91273141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36429203-A-G

91273175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36429252-C-T

91273368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36429379-G-C

91273368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36429379-G-T

91277295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36432182-G-A

91277323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36432211-G-A

91277416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36432313-T-C

91277579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36432489-T-G

91278185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36432940-C-G

91278185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36432940-C-T

91278235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36432987-A-G

91278235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36432987-A-T

91278255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: intron variant
orthologous variants: 36433007-T-G

http://identifiers.org/hco/10/GRCh38#91278335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36433084-C-A

91278335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36433084-C-T

91278413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36433161-A-G

91278483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36433228-A-G

91278533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36433277-A-G

http://identifiers.org/hco/10/GRCh38#91278560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36433305-C-A

91278560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36433305-C-T

91278695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36433437-C-T

91279085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36433834-T-G

91279429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36434138-G-T

http://identifiers.org/hco/10/GRCh38#91279701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36434432-A-C

http://identifiers.org/hco/10/GRCh38#91280440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36435102-A-C

91280440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36435102-A-G

91280440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36435102-A-T

91280635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36435254-T-C

http://identifiers.org/hco/10/GRCh38#91281096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36435652-C-A

91281186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36435704-T-A

91281276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36435782-T-A

91281626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36436116-A-G

http://identifiers.org/hco/10/GRCh38#91281705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36436196-C-A

91281792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36436276-A-G

91281999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36436506-A-G

91282105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36436585-G-T

91282112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36436592-T-C

91282112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36436592-T-G

http://identifiers.org/hco/10/GRCh38#91282780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36436976-A-C

91282912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36437080-T-A

91282954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36437117-A-G

91282997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36437161-C-T

91283018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36437183-C-T

91283137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36437305-T-C

http://identifiers.org/hco/10/GRCh38#91283171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36437340-C-A

91283418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36437536-A-G

http://identifiers.org/hco/10/GRCh38#91283526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#36437634-C-A

91283528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36437636-A-G

91283550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36437651-T-G

91283555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36437656-A-G

91283594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36437697-T-C

91283594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36437697-T-G

91283707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36437817-A-G

91284216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36438324-A-G

91284216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36438324-A-T

91284257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28264
most severe consequence: 3 prime UTR variant
orthologous variants: 36438364-A-G