http://identifiers.org/hco/1/GRCh38#40350343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120881553-C-A

40350396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120881490-G-A

40350449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120881432-G-A

40350449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120881432-G-T

40350487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120881389-G-A

http://identifiers.org/hco/1/GRCh38#40350499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120881377-A-C

40350618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120881274-A-G

40361956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120879421-G-T

40362110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120879323-G-C

40362126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120879308-A-G

40362143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120879305-C-T

http://identifiers.org/hco/1/GRCh38#40362241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120879208-C-A

40362278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120879178-A-G

40362300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 120879156-C-T

40362385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, missense_variant
orthologous variants: 120879076-T-A

40362771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120878432-C-T

40364018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: -C-G

40364018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: -C-T

40371653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120876754-C-T

40371724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120876688-G-A

40371724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120876688-G-C

40371822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120876590-T-C

40372501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120875989-A-T

40373080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120875082-G-T

40373145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120874989-G-A

40373145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120874989-G-T

40373270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120874879-G-A

http://identifiers.org/hco/1/GRCh38#40373558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120874584-C-A

40373558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120874584-C-G

40373558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120874584-C-T

http://identifiers.org/hco/1/GRCh38#40373567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120874577-C-A

40373567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120874577-C-T

http://identifiers.org/hco/1/GRCh38#40373579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120874565-A-C

40373594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120874550-C-T

40373612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120874533-G-T

40373648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120874497-G-A

40373648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120874497-G-T

40373653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120874492-G-T

40373783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120874366-G-A

40373787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120874362-A-G

40373821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120874326-G-A

40373821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120874326-G-C

40373821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120874326-G-T

40373884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120874267-C-T

40373893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120874258-G-A

40373942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120874201-G-A

40374037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120874131-G-A

40374037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120874131-G-C

40374037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120874131-G-T

40374548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120873595-G-A

40374548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120873595-G-T

40374628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120873543-A-T

40374644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120873541-T-A

40374644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120873541-T-G

40374675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120873519-G-A

40374675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120873519-G-T

40374822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120873372-A-G

40374841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120873350-C-G

40374873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120873319-G-A

40374898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120873303-T-C

40374933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120873268-T-C

40374933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120873268-T-G

40375468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120872866-A-G

40375760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120872594-G-A

http://identifiers.org/hco/1/GRCh38#40375851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120872523-C-A

40375851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120872523-C-T

http://identifiers.org/hco/1/GRCh38#40375908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120872468-C-A

http://identifiers.org/hco/1/GRCh38#40375926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120872450-A-C

40376435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120872089-G-A

40376466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120872059-A-T

40378395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120870374-C-T

40378797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120870137-A-G

40380072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120868727-T-G

40382452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120866249-G-A

40382623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 120866113-A-G

40383222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120864725-G-A

40383222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120864725-G-C

40383239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120864708-C-T

40383276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120864672-G-A

40383773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120864327-T-G

40384397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120864070-G-A

http://identifiers.org/hco/1/GRCh38#40384513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120863961-C-A

40384611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120863862-G-C

40384877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120863297-C-T

40385041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 120863135-C-T

40385206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120862980-G-C

40385876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120861931-G-A

40386382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120861154-A-G

40386424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120861116-T-C

40386507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120861035-T-C

40386719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120860818-T-C

40386740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120860800-G-T

40389250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120860081-A-G

40389412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120859926-A-G

http://identifiers.org/hco/1/GRCh38#40390039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120859354-A-C

40390039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120859354-A-G

40390052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120859341-C-T

40390159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120859242-T-C

40390787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120858705-C-G

40391209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120857733-G-A

40391289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120857648-A-T

40391418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120857521-C-T

40391541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120857414-T-C

40392335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120856612-A-G

40392419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120856524-G-C

http://identifiers.org/hco/1/GRCh38#40392661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120856272-A-C

40394428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120853536-T-G

40394753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120853165-A-G

40394807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120853110-T-A

40394913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120853005-G-A

40395743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120851906-G-A

http://identifiers.org/hco/1/GRCh38#40395746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120851903-A-C

40396047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120851397-C-T

40396049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120851395-T-C

40396518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120850477-A-G

40396682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120850322-T-C

40399830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120847808-T-A

40399945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120847717-A-G

40400096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120847536-A-T

40400147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120847489-T-G

40400731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120847173-A-G

40400752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120847152-A-G

40400782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120847123-G-A

http://identifiers.org/hco/1/GRCh38#40400908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120846974-C-A

40401499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120846440-T-C

40401699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120846116-G-A

40401971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845876-A-G

40402889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845715-C-T

40403378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845388-G-A

40403412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845355-C-G

40403412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845355-C-T

http://identifiers.org/hco/1/GRCh38#40403433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120845341-A-C

40403435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845339-A-G

40403459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845327-C-T

40403536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845256-G-A

40403570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845228-T-G

40403618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845181-C-T

40403633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845169-T-C

40403654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845148-G-A

40403730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 120845072-A-G

http://identifiers.org/hco/1/GRCh38#40403768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120845038-A-C

40403772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120845034-A-G

40404186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120844842-T-C

40404574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120844374-T-C

40404644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120844150-T-C

40404658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120844124-C-G

40404874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120843925-G-A

40404878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120843921-C-G

40405017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120843800-G-A

40405017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120843800-G-T

40405098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120843720-A-G

40405573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120843609-C-T

40405690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120843502-G-A

40405707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120843485-T-C

http://identifiers.org/hco/1/GRCh38#40405967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120843227-C-A

40406163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120843062-G-A

40406179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120843054-C-T

40406331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120842913-C-T

40406440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120842805-G-A

40406490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120842757-C-G

http://identifiers.org/hco/1/GRCh38#40406612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120842631-C-A

http://identifiers.org/hco/1/GRCh38#40406637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120842609-C-A

40406657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120842590-T-C

40406657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120842590-T-G

40406684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120842564-G-A

40406684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120842564-G-C

40406689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120842559-T-C

40406895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120842365-T-A

40408101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120841371-T-C

40408542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120840492-T-C

40408542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120840492-T-G

40408600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120840438-T-C

40408707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: missense variant
orthologous variants: 120840333-C-T

40408837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120840210-A-G

40409081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120839980-G-A

40410060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120839063-A-T

40410095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120839002-T-C

40410392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120838437-T-C

40410397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120838432-T-C

40410692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120838165-T-C

40410987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120837905-T-C

40411689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120836302-A-T

40413112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120834136-G-A

40413112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120834136-G-T

http://identifiers.org/hco/1/GRCh38#40413124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120834126-C-A

40413124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120834126-C-T

40413138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120834112-T-C

40413185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120834057-G-A

40413185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120834057-G-T

40413257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120833995-G-C

40413444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120833395-C-T

40413610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120833295-A-T

40413976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120832812-T-A

40413976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120832812-T-G

40414207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120832600-T-C

40414345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120832466-G-A

http://identifiers.org/hco/1/GRCh38#40414510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120832331-A-C

40414510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120832331-A-G

40414750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120832123-T-C

http://identifiers.org/hco/1/GRCh38#40415173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120831761-C-A

http://identifiers.org/hco/1/GRCh38#40415463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120831505-C-A

40415463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120831505-C-G

40415463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120831505-C-T

40415513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120831461-T-A

http://identifiers.org/hco/1/GRCh38#40415515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120831459-A-C

40415515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120831459-A-G

40415555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120831421-T-C

40415706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120831273-G-A

40415842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120831159-C-T

40416027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120830849-T-C

http://identifiers.org/hco/1/GRCh38#40416054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120830818-C-A

40416054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120830818-C-T

http://identifiers.org/hco/1/GRCh38#40416117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120830596-C-A

40416117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120830596-C-G

http://identifiers.org/hco/1/GRCh38#40416265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120830364-A-C

40416381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120830249-A-G

40416492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120829659-G-A

40416492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120829659-G-T

40416498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120829654-A-T

http://identifiers.org/hco/1/GRCh38#40416604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120829547-C-A

40416839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: missense variant
orthologous variants: 120829342-G-T

http://identifiers.org/hco/1/GRCh38#40417253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120828946-A-C

40417253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120828946-A-T

40417284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120828924-G-T

40417493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120828761-C-T

40417520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120828732-G-A

40417596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120828673-A-G

40420952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120827836-G-A

40420952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120827836-G-T

40421264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron variant
orthologous variants: 120827526-A-G

http://identifiers.org/hco/1/GRCh38#40421901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120826920-A-C

40421901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: intron_variant, undefined
orthologous variants: 120826920-A-G

http://identifiers.org/hco/1/GRCh38#40422160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120826675-C-A

40422160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826675-C-T

40422163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 120826672-C-T

40422200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826633-T-A

40422298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826529-G-A

40422298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826529-G-C

http://identifiers.org/hco/1/GRCh38#40422303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120826525-A-C

40422303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826525-A-G

40422303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826525-A-T

40422417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826402-A-G

40422425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826394-A-G

40422432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826387-G-A

40422432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826387-G-T

40422456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826363-G-A

40422456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826363-G-T

40422459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826360-G-C

40422459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826360-G-T

http://identifiers.org/hco/1/GRCh38#40422770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120826044-C-A

40422770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826044-C-T

40422791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120826024-T-C

40423050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120825783-A-G

40423076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25082
most severe consequence: 3 prime UTR variant
orthologous variants: 120825757-C-T