44911335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116693726-G-A

44911335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116693726-G-T

44911364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116693697-G-T

44911469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116693580-T-A

44911469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116693580-T-G

44911471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116693578-T-G

44911625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693423-C-G

44911625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693423-C-T

44911630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693418-G-C

44911630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693418-G-T

44911665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693383-G-A

44911665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693383-G-C

44911665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693383-G-T

http://identifiers.org/hco/10/GRCh38#44911729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116693319-C-A

44911729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693319-C-G

44911729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693319-C-T

44911797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116693253-T-C

http://identifiers.org/hco/10/GRCh38#44912329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116692786-C-A

44912448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692669-C-G

44912645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692476-C-T

44912683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692455-G-A

44912777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692378-G-A

44912903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692264-G-C

44912962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692209-G-T

44913121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692129-T-C

44913135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692116-G-A

44913208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692074-C-T

44913243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116692014-T-G

44913272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116691971-C-T

44913458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116691815-A-G

44913461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116691812-C-G

http://identifiers.org/hco/10/GRCh38#44913494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116691791-A-C

44913494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116691791-A-G

44913559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116691726-G-T

http://identifiers.org/hco/10/GRCh38#44916223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116690253-C-A

44916567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116689673-T-A

44916715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116689541-C-T

44916787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116689487-T-C

44916847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116689427-C-T

44917417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116688991-G-A

http://identifiers.org/hco/10/GRCh38#44917422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116688986-A-C

44917422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116688986-A-T

44919790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116680106-T-C

http://identifiers.org/hco/10/GRCh38#44919804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116680092-A-C

http://identifiers.org/hco/10/GRCh38#44919853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116680043-C-A

44919853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116680043-C-T

44919874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116680023-T-C

44919897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116680000-T-A

44919897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116680000-T-C

44919897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116680000-T-G

44919924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116679986-T-C

44919924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116679986-T-G

44927811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679110-G-A

44927811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679110-G-T

44927814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679107-G-A

44927814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679107-G-T

44927815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679106-T-C

44927833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679089-A-G

44927833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679089-A-T

44927875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679049-G-C

44927890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679033-G-A

44927896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116679027-T-C

44927988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116678935-G-A

44927988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116678935-G-T

44928006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678922-G-A

44928006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678922-G-T

44928011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678917-T-C

http://identifiers.org/hco/10/GRCh38#44928082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116678849-C-A

44928082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678849-C-T

44928108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678824-G-A

44928109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678823-G-A

44928109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678823-G-T

44928675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678509-C-T

44928679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678505-C-T

44929080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678242-G-A

44929093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678230-T-G

http://identifiers.org/hco/10/GRCh38#44929466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116677931-C-A

44929466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677931-C-G

44929466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677931-C-T

44929515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677888-T-C

44929542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677860-G-A

44929565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677837-G-A

http://identifiers.org/hco/10/GRCh38#44929569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116677833-C-A

44929569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677833-C-T

44929818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677679-G-A

44929818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677679-G-C

44929818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677679-G-T

44929844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677662-C-T

44930313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677308-T-C

44930387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677231-G-A

44930428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677188-C-T

44930683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676984-G-A

44930750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676927-T-C

44930846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676827-G-A

44930846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676827-G-C

44930910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676754-T-C

44931012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676658-G-A

44931230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676476-G-A

44931231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676475-G-A

44931500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676103-G-A

44931500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676103-G-T

44931592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675896-C-G

44931703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675640-T-C

44931708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675636-G-T

44931714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675630-G-A

44931714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675630-G-C

44931714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675630-G-T

44931736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675607-G-C

44931736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675607-G-T

44931752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675591-G-A

44931752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675591-G-T

http://identifiers.org/hco/10/GRCh38#44931760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116675583-C-A

44931760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675583-C-T

44931768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675575-G-A

44931768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675575-G-T

44931858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675511-T-G

44931859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675510-G-A

44931859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675510-G-T

44931892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675457-C-T

44931893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675456-A-G

44931894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675455-T-C

44931937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675413-G-A

44931962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675389-G-A

44931962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675389-G-T

44931964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116675387-G-A

44932092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675256-C-T

44932208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675149-T-A

44932208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675149-T-C

http://identifiers.org/hco/10/GRCh38#44932538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116674901-C-A

44932570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674881-C-T

http://identifiers.org/hco/10/GRCh38#44932616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116674823-C-A

44932616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674823-C-T

44932639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674798-G-A

44932644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674793-T-C

44932878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116674570-G-A

44933227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116674304-A-T

http://identifiers.org/hco/10/GRCh38#44933490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116674082-C-A

44933490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674082-C-T

44933521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674033-G-A

44933521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674033-G-T

http://identifiers.org/hco/10/GRCh38#44933561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116673991-C-A

44933561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673991-C-T

http://identifiers.org/hco/10/GRCh38#44933570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116673980-C-A

44933570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673980-C-T

44933572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673978-T-C

44933644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116673898-C-T

http://identifiers.org/hco/10/GRCh38#44933657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116673885-C-A

44933659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116673883-G-T

44933789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673752-G-A

44933789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673752-G-C

44933831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673707-G-C

44933831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673707-G-T

44933903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673656-G-A

44933903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673656-G-T

44933964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673607-G-A

44934022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673551-G-A

44934234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116673369-A-G

http://identifiers.org/hco/10/GRCh38#44934551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116672594-C-A

44934551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672594-C-T

44934568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672577-G-T

44934571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672574-G-T

44934577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672568-C-G

44934581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672564-T-C

44934600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672549-G-A

44934600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672549-G-T

44934602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672547-C-T

44934603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672546-T-A

44934603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672546-T-C

44934636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116672509-G-T

http://identifiers.org/hco/10/GRCh38#44934719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116672425-C-A

http://identifiers.org/hco/10/GRCh38#44934769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116672375-A-C

44934853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116672291-T-C

44934853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116672291-T-G

http://identifiers.org/hco/10/GRCh38#44934973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116672171-C-A

44934973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116672171-C-T

44934995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116672149-G-A

44935064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116672080-C-T

44935226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671911-T-C

44935240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671910-G-A

44935240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671910-G-C

http://identifiers.org/hco/10/GRCh38#44935252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116671898-C-A

44935288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671862-G-A

44935318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671835-G-T

44935368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671792-T-C

http://identifiers.org/hco/10/GRCh38#44935372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116671788-C-A

44935416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671763-G-A

44935416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671763-G-T

44935428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671751-G-A

http://identifiers.org/hco/10/GRCh38#44935432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116671747-C-A

44935459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671720-A-G

44935459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671720-A-T

44935506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671691-T-A

44935506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671691-T-G

http://identifiers.org/hco/10/GRCh38#44935549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116671631-C-A

44935549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671631-C-T

44935575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671602-T-C

44935719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671494-G-A

44935719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116671494-G-T

44935849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671328-T-C

44935861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671307-A-G

44935887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671254-G-A

44935887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671254-G-T

44935898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671243-G-A

44935898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671243-G-T

44935916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671225-A-G

44935927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671212-G-A

44935927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671212-G-T

http://identifiers.org/hco/10/GRCh38#44935977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116671160-C-A

44935977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671160-C-T

http://identifiers.org/hco/10/GRCh38#44935978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116671159-A-C

44936057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671086-G-T

44936066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671077-G-A

44936066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671077-G-T

44936078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671065-C-T

44936089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116671054-G-C

44936282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116670882-A-G

44936321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116670847-G-T

44936361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116670801-A-G

44936402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116670771-C-T

http://identifiers.org/hco/10/GRCh38#44936453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116670679-C-A

44936478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116670654-G-A

http://identifiers.org/hco/10/GRCh38#44936489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116670644-C-A

44936527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116670614-C-T

http://identifiers.org/hco/10/GRCh38#44936655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116670469-C-A

44936655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31658
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116670469-C-T