31291832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51922696-T-C

31291926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51922791-T-C

31292008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51922875-C-T

http://identifiers.org/hco/14/GRCh38#31292015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51922882-C-A

31292062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51922925-A-G

http://identifiers.org/hco/14/GRCh38#31292289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51923128-C-A

31292289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51923128-C-T

31292448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51923274-C-T

31292476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51923301-A-G

31292482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51923307-T-C

31292651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51923402-T-A

31292651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51923402-T-C

31292739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51923490-C-T

31292783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51923563-A-G

http://identifiers.org/hco/14/GRCh38#31292826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51923628-C-A

31292826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51923628-C-T

http://identifiers.org/hco/14/GRCh38#31292827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51923629-C-A

31292827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51923629-C-G

31292827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51923629-C-T

31293029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51923847-G-A

http://identifiers.org/hco/14/GRCh38#31293197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#51923987-A-C

http://identifiers.org/hco/14/GRCh38#31293203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51923993-C-A

31293528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51924315-A-G

31293629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51924413-T-C

31293630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51924414-A-G

31293650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51924433-A-T

31293972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51926119-C-T

http://identifiers.org/hco/14/GRCh38#31293997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51926144-C-A

31294009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 51926156-G-T

31294039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 51926186-G-A

31294098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51926245-T-A

31294098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51926245-T-C

31294157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51926323-G-T

31294229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51926390-A-G

31294229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51926390-A-T

31294790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51926598-G-A

31295128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51926916-C-T

31295888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51927876-T-C

31295888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51927876-T-G

31295922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51927910-A-T

http://identifiers.org/hco/14/GRCh38#31296059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51928044-A-C

31296059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 51928044-A-G

31296059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51928044-A-T

31296076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51928061-G-T

31296083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51928067-T-A

31296102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51928084-C-T

31296110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51928092-T-A

31296110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51928092-T-C

31296127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51928107-G-A

31296127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51928107-G-T

31297801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51929594-C-T

31297868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51929662-G-T

31297870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51929664-G-A

31297870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51929664-G-T

31297911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51929714-A-G

31298012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51929794-G-A

31298079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51929857-A-G

http://identifiers.org/hco/14/GRCh38#31302230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51930983-C-A

31302230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51930983-C-T

31302314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51931069-A-G

31302320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51931075-T-C

31302380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51931135-G-C

31302410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51931165-T-A

31302410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51931165-T-C

31302560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51931308-T-C

31302570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51931314-G-A

31302570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51931314-G-T

http://identifiers.org/hco/14/GRCh38#31302589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51931328-C-A

31302589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51931328-C-G

31302691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51932152-G-A

31302691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51932152-G-C

31302691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51932152-G-T

31304760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51934388-T-C

31304835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51934440-C-G

31304954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51934830-T-C

31305008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51934884-T-G

31305082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51934958-T-C

31305561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51935122-C-T

31305783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51935345-C-T

http://identifiers.org/hco/14/GRCh38#31306957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51935876-C-A

http://identifiers.org/hco/14/GRCh38#31308037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51936514-A-C

31309045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51938119-A-G

31309048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51938122-C-T

31309049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51938123-T-G

http://identifiers.org/hco/14/GRCh38#31309139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51938207-C-A

31309139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51938207-C-T

31309177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51938245-C-T

http://identifiers.org/hco/14/GRCh38#31309317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51938323-C-A

31309317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938323-C-T

31309318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938324-T-A

31309318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938324-T-C

31309401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938390-T-C

31309720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938748-T-C

31309858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938849-A-G

31309891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938882-T-C

31309919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938910-T-C

31309945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938927-T-C

31309966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938947-G-C

31309983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938964-G-A

31309994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938976-C-T

31309995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51938977-G-A

31313053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51940518-T-C

31313053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51940518-T-G

31313086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51940551-T-G

31315863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51941139-A-G

31315872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51941148-T-C

31315872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51941148-T-G

31318230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51943352-T-C

31318332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51943454-A-G

31318423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51943528-G-A

31318423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51943528-G-T

31318870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51943636-C-G

31319048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51943783-G-A

31319154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51943879-T-C

31319157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51943882-T-G

31320996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51944425-G-A

31321493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51944524-G-A

31321493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51944524-G-T

31321577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51944608-T-C

31321676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51944707-G-T

http://identifiers.org/hco/14/GRCh38#31321740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51944753-C-A

http://identifiers.org/hco/14/GRCh38#31321746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51944759-C-A

31321766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51944779-T-C

http://identifiers.org/hco/14/GRCh38#31321790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51944805-C-A

http://identifiers.org/hco/14/GRCh38#31321794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51944809-C-A

31321794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51944809-C-T

31321804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51944819-T-C

31322136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51945178-A-G

31322164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51945206-T-C

http://identifiers.org/hco/14/GRCh38#31323516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51945801-C-A

31323516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51945801-C-G

31323516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51945801-C-T

31323553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51945826-T-C

http://identifiers.org/hco/14/GRCh38#31323576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51945849-C-A

31323576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51945849-C-T

http://identifiers.org/hco/14/GRCh38#31323617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51945890-A-C

31323737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51946007-T-C

31323826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946095-T-C

31323828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946096-T-A

31323828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946096-T-C

31323870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946130-G-A

31323870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946130-G-C

31323870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946130-G-T

31323947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946196-C-G

31323947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946196-C-T

http://identifiers.org/hco/14/GRCh38#31323950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51946199-C-A

31323950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946199-C-T

31323953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946202-A-G

31324065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946282-C-T

31324315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946509-G-A

31324414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51946701-T-C

31325736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51951630-A-G

http://identifiers.org/hco/14/GRCh38#31325775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51951660-C-A

31325813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51951697-G-T

31326007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 51951956-C-T

http://identifiers.org/hco/14/GRCh38#31326078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51952021-C-A

31326078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 51952021-C-T

31326087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 51952030-T-C

31326092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, missense_variant
orthologous variants: 51952035-G-T

31326127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 51952068-A-G

31326128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 51952069-T-C

31326128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, missense_variant
orthologous variants: 51952069-T-G

31326197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51952138-T-G

31326230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51952171-T-C

31326230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51952171-T-G

31326231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51952172-G-A

31326245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51952186-T-G

31326284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51952225-C-T

31326396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, undefined
orthologous variants: 51952331-T-A

http://identifiers.org/hco/14/GRCh38#31326406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51952341-A-C

31326444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51952382-A-G

31326456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51952393-T-A

31326456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51952393-T-C

31326465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51952402-T-C

http://identifiers.org/hco/14/GRCh38#31326476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51952412-A-C

31326532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51952471-T-C

31337459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51956724-T-C

31337584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: stop gained
orthologous variants: 51956846-T-A

31337584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51956846-T-C

31337754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51957011-T-A

31337754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51957011-T-C

31337754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51957011-T-G

31337848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51957106-C-T

31338005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51957213-A-G

31338021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51957233-T-C

31338025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51957237-G-C

31338694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51958026-T-C

31339837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51958393-T-C

31339947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51958501-A-G

31340008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51958561-A-G

31340043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51958591-C-T

31340069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51958615-T-G

31340083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51958629-T-C

31340177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51958723-T-C

http://identifiers.org/hco/14/GRCh38#31340370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51958911-C-A

31340370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51958911-C-T

http://identifiers.org/hco/14/GRCh38#31340379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51958920-C-A

31340379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51958920-C-G

http://identifiers.org/hco/14/GRCh38#31340390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51958930-C-A

31340390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51958930-C-T

http://identifiers.org/hco/14/GRCh38#31340468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51959006-C-A

31340468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 51959006-C-T

31340472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, missense_variant
orthologous variants: 51959010-A-G

http://identifiers.org/hco/14/GRCh38#31340499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51959037-C-A

31340501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51959039-A-G

31340507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51959045-G-T

http://identifiers.org/hco/14/GRCh38#31340514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51959053-C-A

http://identifiers.org/hco/14/GRCh38#31340546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51959084-C-A

31340546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51959084-C-T

31340894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51959408-C-G

31341728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51959966-G-C

31342007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51960221-T-C

31342511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51960346-C-T

31343589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51961469-C-T

31343664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51961548-A-G

31343690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51961577-G-C

http://identifiers.org/hco/14/GRCh38#31343834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51961707-C-A

31343834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51961707-C-T

31344034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51961895-A-G

31344084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51961945-A-G

31344085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51961946-G-A

31344085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51961946-G-T

31344916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51962680-T-C

31344938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51962702-G-T

31344985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51962748-C-T

31344987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51962750-T-C

31345006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51962771-C-T

31345221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51962984-T-C

31345290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51963053-G-A

31345290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51963053-G-C

31345290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51963053-G-T

31347564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51965195-A-G

31347730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51965349-A-G

http://identifiers.org/hco/14/GRCh38#31347993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51965923-C-A

31347993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51965923-C-G

31347993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51965923-C-T

31348046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51965975-T-A

31348046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51965975-T-C

31348068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51965998-C-T

http://identifiers.org/hco/14/GRCh38#31348070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51966000-A-C

31348236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51966318-T-C

31349752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51967143-A-T

31349780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51967164-T-C

31349802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51967186-C-T

31349812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51967196-T-C

31349828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51967212-C-T

31349845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51967229-G-A

31349845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51967229-G-C

31349845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51967229-G-T

31349926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51967310-G-A

http://identifiers.org/hco/14/GRCh38#31349962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51967343-C-A

31349962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51967343-C-T

31350007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51967388-T-A

31350016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51967397-T-A

31350016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51967397-T-C

31350035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51967416-G-A

31350035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51967416-G-T

31358744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51971888-A-G

31358987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51972130-A-G

http://identifiers.org/hco/14/GRCh38#31359003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51972146-A-C

31359003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51972146-A-G

31359005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51972148-A-G

31359005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51972148-A-T

31359014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51972157-A-T

31359020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51972163-G-A

31359045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51972188-G-A

31359046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51972189-C-G

31359046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51972189-C-T

http://identifiers.org/hco/14/GRCh38#31359108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51972253-A-C

31359152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51972298-G-A

31359152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51972298-G-T

31359184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51972327-T-C

31359289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51972433-T-A

31359544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51972674-T-C

31359636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51972825-A-G

31359657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51972870-C-T

31359708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51972917-G-A

31359708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51972917-G-C

31359708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51972917-G-T

http://identifiers.org/hco/14/GRCh38#31359752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51972978-A-C

http://identifiers.org/hco/14/GRCh38#31359765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51972991-A-C

31359765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51972991-A-G

31360028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51973224-C-T

http://identifiers.org/hco/14/GRCh38#31360110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51973297-C-A

31360133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51973316-G-T

31361580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51973913-C-T

31361717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51973938-T-G

31361728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51973949-A-G

31362387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: -T-G

31364126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51976914-A-G

31364213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51976998-A-G

31364358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51977142-T-C

31364358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51977142-T-G

31366499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51977786-G-C

31366690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51977960-C-T

http://identifiers.org/hco/14/GRCh38#31371476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51984522-C-A

31371484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51984530-T-C

31371513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51984546-G-A

31371513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51984546-G-T

http://identifiers.org/hco/14/GRCh38#31371669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51984695-C-A

31371669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51984695-C-T

31371697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51984732-T-C

http://identifiers.org/hco/14/GRCh38#31371726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51984758-C-A

http://identifiers.org/hco/14/GRCh38#31371740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51984772-C-A

31371740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51984772-C-G

31371740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51984772-C-T

31371750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51984782-T-A

31371750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51984782-T-C

http://identifiers.org/hco/14/GRCh38#31371772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51984801-C-A

31371772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51984801-C-T

31371843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51984887-G-A

31371843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51984887-G-T

31371851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51984895-A-G

31371869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51984913-A-G

31371869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51984913-A-T

http://identifiers.org/hco/14/GRCh38#31371880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51984924-C-A

31371880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51984924-C-T

31371890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51984934-G-A

31371890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51984934-G-C

31371890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51984934-G-T

31371956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51985001-T-A

31371956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51985001-T-C

31371956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51985001-T-G

31372025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51985060-A-G

31372031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51985066-A-T

31372169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51985186-C-G

31372169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51985186-C-T

http://identifiers.org/hco/14/GRCh38#31374691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51986251-A-C

31374691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51986251-A-G

http://identifiers.org/hco/14/GRCh38#31374717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51986271-C-A

31374717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51986271-C-T

http://identifiers.org/hco/14/GRCh38#31374743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51986297-C-A

31374751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51986302-T-C

31374763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51986309-A-G

31374763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51986309-A-T

http://identifiers.org/hco/14/GRCh38#31374793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51986331-A-C

31374873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 51986411-G-A

31374873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51986411-G-T

31374877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51986415-C-T

31374941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51986479-G-C

31374949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51986487-A-G

31375012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51986525-G-A

31375012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51986525-G-T

31375044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51986557-A-G

31375044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51986557-A-T

31375060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51986580-T-A

31375060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51986580-T-C

31375075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51986595-G-A

31375075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51986595-G-C

31375075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51986595-G-T

31375644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51987692-C-T

31375684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51987730-G-C

31375688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51987734-C-T

31375740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51987777-C-T

31375758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51987795-A-G

31375760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51987811-A-G

31375823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51987902-G-A

31376038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51988364-C-T

31376115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51988449-G-A

http://identifiers.org/hco/14/GRCh38#31376136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51988469-C-A

31376215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51988544-T-C

31376219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51988548-C-T

31376221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51988550-G-A

31378071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, undefined
orthologous variants: 51990902-G-A

31378525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991245-C-T

31378535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991255-C-T

31378562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991281-T-A

31378585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991297-A-G

31378588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991300-C-T

31378609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991350-A-G

31379554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991450-C-G

31380032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991604-T-G

31380157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991735-G-A

31380157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991735-G-C

31380275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991844-G-A

31380275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991844-G-C

31380298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991868-G-A

31380316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51991901-T-G

http://identifiers.org/hco/14/GRCh38#31380413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51992149-C-A

31380414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992150-A-G

31380414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992150-A-T

http://identifiers.org/hco/14/GRCh38#31380436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51992171-C-A

31380436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992171-C-T

31380437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992172-A-G

31380437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992172-A-T

http://identifiers.org/hco/14/GRCh38#31380460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51992197-C-A

31380460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 51992197-C-T

31380543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51992280-A-T

31380584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 51992321-T-A

31380584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 51992321-T-C

31380663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992395-T-C

31380664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992396-T-A

31380664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992396-T-C

31380706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992431-T-C

31380710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992435-T-C

31380718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992443-A-G

31380724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992449-T-C

31380724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992449-T-G

http://identifiers.org/hco/14/GRCh38#31380737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51992464-A-C

31380816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992542-T-C

31380818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992544-G-C

http://identifiers.org/hco/14/GRCh38#31380871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51992596-A-C

31380871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51992596-A-G

31382977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993457-G-A

31382981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993461-C-T

31383008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993488-G-C

31383012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993492-C-T

31383047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993534-T-A

31383070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993557-C-T

31383102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993589-T-C

31383149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993640-A-G

31383174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993658-T-C

31383214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993880-T-C

31383224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993890-C-T

31383298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993954-A-G

31383310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51993966-A-G

31383346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994021-T-C

31383404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994219-T-C

31383405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994220-A-T

31383408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994223-G-A

31383408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994223-G-T

31383462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994257-G-A

31383462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994257-G-T

31383464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994259-G-T

31383553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51994570-A-G

31383569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51994586-C-T

31383578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51994595-T-G

http://identifiers.org/hco/14/GRCh38#31383584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51994601-A-C

31383584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51994601-A-G

31383597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51994614-C-T

31383632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51994649-A-T

31383636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51994653-C-T

31383671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51994688-G-A

31383674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51994691-G-C

31383718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51994735-G-A

http://identifiers.org/hco/14/GRCh38#31383720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51994737-C-A

31383720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51994737-C-T

31383749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51994766-T-C

31383749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51994766-T-G

31383797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994816-T-C

http://identifiers.org/hco/14/GRCh38#31383803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51994822-C-A

31383803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994822-C-T

31383807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994826-G-T

http://identifiers.org/hco/14/GRCh38#31383884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51994917-C-A

31383891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994924-T-A

31383899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994932-A-T

http://identifiers.org/hco/14/GRCh38#31383904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51994935-C-A

31383904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994935-C-T

31383978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994969-C-T

31383989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51994980-C-G

31384034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51995023-G-A

31384857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51995414-T-G

31384896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51995454-C-G

31384943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51995493-G-A

31384969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51995513-G-C

31385013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51995556-T-G

31385033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51995576-A-G

31386075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51995986-A-G

31386087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51995998-G-C

31386290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51996575-A-G

31386290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51996575-A-T

http://identifiers.org/hco/14/GRCh38#31386335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51996622-A-C

31386335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51996622-A-G

31386350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51996651-G-A

31386350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51996651-G-T

31386352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51996653-A-G

31386373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51996675-A-G

http://identifiers.org/hco/14/GRCh38#31386396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51996698-C-A

31386396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51996698-C-T

31386436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51996731-T-C

31386445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51996740-T-C

31386463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51996758-A-G

31386464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51996759-T-C

31386493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51996788-A-G

http://identifiers.org/hco/14/GRCh38#31386502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51996797-C-A

31386502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51996797-C-G

31386507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 51996802-T-C

31386520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51996815-G-A

31386552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 51996847-A-G

31386604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51996899-A-G

31386655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51996952-T-A

31386655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51996952-T-C

31386668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51996964-T-C

31386698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51997010-T-A

31386698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51997010-T-C

31386698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51997010-T-G

31386711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51997023-T-A

31386711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51997023-T-C

31387033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51997618-A-T

31387044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51997643-A-G

31387076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51997672-T-C

http://identifiers.org/hco/14/GRCh38#31387085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51997679-A-C

31387085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51997679-A-G

31387092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51997687-A-G

31387116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51997708-A-G

31387145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 51997737-G-A

31387383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 51997974-G-A

31387383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 51997974-G-C

31387679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51998086-C-T

31387682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51998089-C-G

31387684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51998091-C-T

31387922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51998206-G-C

31388114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51998434-T-C

31388282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51998753-C-T

31388411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51998886-T-A

31388432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51998903-T-C

31388468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51998936-T-C

31388487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51998954-A-G

31388553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51999002-T-A

31388641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51999087-C-T

http://identifiers.org/hco/14/GRCh38#31388711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51999155-C-A

31388711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51999155-C-G

31388711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51999155-C-T

31388735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51999173-G-T

http://identifiers.org/hco/14/GRCh38#31389032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51999457-C-A

31389032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51999457-C-T

31389036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51999461-T-A

31389036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51999461-T-C

31389060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51999741-A-G

http://identifiers.org/hco/14/GRCh38#31389138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#51999814-C-A

31389138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51999814-C-G

31389138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 51999814-C-T

31389170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, undefined
orthologous variants: 51999850-G-A

http://identifiers.org/hco/14/GRCh38#31393933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52002067-C-A

31393933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52002067-C-T

31394005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52002120-G-A

31394005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52002120-G-T

31394015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52002130-T-A

31394015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52002130-T-C

31394065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 52002176-T-C

31394149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 52002260-C-G

31394149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 52002260-C-T

31394178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 52002289-G-T

31394231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 52002342-T-A

31394231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 52002342-T-C

31394297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52002407-G-A

31394297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52002407-G-T

31394356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52002455-A-G

31394428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52002503-G-C

31394440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52002515-C-G

31394496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52002577-A-G

31395391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003093-T-A

31395402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003110-G-A

31395402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003110-G-T

http://identifiers.org/hco/14/GRCh38#31395448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52003152-C-A

http://identifiers.org/hco/14/GRCh38#31398554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52003758-A-C

31398554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003758-A-G

31398557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003761-T-C

31398557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003761-T-G

http://identifiers.org/hco/14/GRCh38#31398573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52003767-C-A

31398573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003767-C-T

31398619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003818-T-C

31398619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003818-T-G

31398653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003852-C-T

31398670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003859-T-A

31398715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 52003904-A-G

31398724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 52003913-G-A

31398788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 52003977-C-G

31398788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 52003977-C-T

31398808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003998-A-G

31398809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003999-G-A

31398809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003999-G-C

31398809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52003999-G-T

31398827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52004017-G-C

31398827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52004017-G-T

31398840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52004033-C-G

31398856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52004050-A-G

31398896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52004093-C-T

31400040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52004477-T-C

31400194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52005531-G-T

http://identifiers.org/hco/14/GRCh38#31400201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52005538-C-A

31400201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52005538-C-T

http://identifiers.org/hco/14/GRCh38#31400205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52005542-C-A

31400357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 52005692-T-C

31400366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 52005701-T-C

31400383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: 52005718-A-G

31400444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 52005779-C-T

http://identifiers.org/hco/14/GRCh38#31400462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52005797-C-A

31400462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: synonymous variant
orthologous variants: 52005797-C-T

http://identifiers.org/hco/14/GRCh38#31400548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52005864-C-A

31400555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52005871-A-G

http://identifiers.org/hco/14/GRCh38#31400570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52005885-C-A

31400635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52005921-T-A

31400750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52006016-G-A

31401803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52006185-T-G

31401945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52006319-T-A

31401992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52006370-T-C

31402371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52007207-T-A

31402422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52007255-A-T

31402695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52008053-G-A

31402846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52008212-C-T

http://identifiers.org/hco/14/GRCh38#31403018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52008390-A-C

31403055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 52008433-A-G

31403072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52008448-A-G

31403087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52008462-T-A

31403171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52008552-A-G

31403352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52008751-G-C

31403530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52008905-C-T

http://identifiers.org/hco/14/GRCh38#31404190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52009413-A-C

31404375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52009571-A-G

31404785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52009832-G-A

31404795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52009834-T-C

31404800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52009839-G-A

31404917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52009941-A-G

31404983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52009997-G-C

31405045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52010064-G-A

http://identifiers.org/hco/14/GRCh38#31405056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52010079-C-A

http://identifiers.org/hco/14/GRCh38#31405081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52010104-C-A

31405081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52010104-C-T

31405860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52010873-G-A

31405933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52010992-T-C

31405955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52011013-T-G

31406046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52011093-G-A

31406047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52011094-C-T

31406170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52011202-T-C

31406277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52011284-C-T

31406315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52011444-G-A

31406413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52011543-T-C

http://identifiers.org/hco/14/GRCh38#31414268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52014461-A-C

31414280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52014473-G-A

31414280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52014473-G-C

31414438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52014635-G-C

31414482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52014695-C-T

31414654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52014857-G-A

31414743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52014944-C-G

http://identifiers.org/hco/14/GRCh38#31415028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52015051-C-A

31415381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52015274-C-G

31418946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52016317-G-A

http://identifiers.org/hco/14/GRCh38#31419190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52016805-C-A

31419238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52016850-T-C

31419522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52017291-T-G

31419661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52017383-G-A

31419784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52017508-C-G

http://identifiers.org/hco/14/GRCh38#31420124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52017746-C-A

31420124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52017746-C-T

31420141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52017756-T-A

31420141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron variant
orthologous variants: 52017756-T-C

31420198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 52017786-G-A

31420198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 52017786-G-T

31420267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52017827-T-C

http://identifiers.org/hco/14/GRCh38#31420285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#52017845-C-A

31420285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52017845-C-T

31420399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 52017937-G-A

31420399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 52017937-G-T

31420456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 52017972-A-G

31420544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 52018054-A-G

31420546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20276
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 52018056-A-G