96955182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6808398-G-T

96955305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6808518-T-A

96955551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6808799-T-C

96955625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6808875-G-T

96955667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6808924-C-T

96955740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6809001-T-C

96955915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6809443-C-T

http://identifiers.org/hco/7/GRCh38#96956270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6809787-C-A

96956270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6809787-C-T

96956464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6811050-G-A

96956464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6811050-G-C

96956464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6811050-G-T

96956662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6811238-T-C

96956727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6811301-C-T

96956729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6811303-A-G

http://identifiers.org/hco/7/GRCh38#96956905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6811495-C-A

http://identifiers.org/hco/7/GRCh38#96956924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6811512-C-A

96956924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6811512-C-G

96956924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6811512-C-T

96956994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6811587-G-A

96956994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6811587-G-T

96957000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6811603-G-T

96957009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6811612-A-G

http://identifiers.org/hco/7/GRCh38#96957448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6812122-C-A

96957618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6812303-G-T

96957654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6812308-G-C

96957654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6812308-G-T

96957659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6812313-T-C

96957957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6812437-G-T

96958170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6812621-G-A

96958289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6812723-A-G

96958289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6812723-A-T

96958345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6812779-A-G

96958345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6812779-A-T

96958399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6812832-G-A

96958399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6812832-G-C

96959053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6813288-G-A

http://identifiers.org/hco/7/GRCh38#96959056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6813291-A-C

96959099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6813334-G-A

96959099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6813334-G-T

96959116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6813351-G-T

96959259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6813700-G-T

http://identifiers.org/hco/7/GRCh38#96959425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6813917-C-A

96959425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6813917-C-T

96959709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6814318-C-G

96959797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6814442-C-T

http://identifiers.org/hco/7/GRCh38#96960255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6814902-C-A

96960316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6814962-G-A

http://identifiers.org/hco/7/GRCh38#96960325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6814976-C-A

96960349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6815011-G-T

96960384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6815046-G-T

http://identifiers.org/hco/7/GRCh38#96960799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6816693-C-A

96960828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6816771-T-A

96960833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6816776-G-A

http://identifiers.org/hco/7/GRCh38#96960838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6816781-C-A

96960845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6816790-G-A

96961081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6817013-A-G

http://identifiers.org/hco/7/GRCh38#96961095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6817027-A-C

http://identifiers.org/hco/7/GRCh38#96961148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6817087-C-A

96961148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6817087-C-G

96961148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6817087-C-T

96962507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818129-C-T

96962525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818146-A-G

http://identifiers.org/hco/7/GRCh38#96962532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6818153-C-A

96962532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818153-C-T

96962567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818188-G-C

96962575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818196-G-T

96962597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818217-G-A

96962597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818217-G-T

96962632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818254-C-T

http://identifiers.org/hco/7/GRCh38#96962653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6818275-C-A

96962653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818275-C-T

96962666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818288-G-A

http://identifiers.org/hco/7/GRCh38#96962721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6818339-C-A

96962721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818339-C-T

96962780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818400-T-A

96963097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818712-T-C

http://identifiers.org/hco/7/GRCh38#96963261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6818868-C-A

96963354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818962-G-A

96963354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6818962-G-T

96963634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6819260-C-T

http://identifiers.org/hco/7/GRCh38#96963718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6819343-C-A

96964081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6819720-T-C

96964321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6819962-T-G

http://identifiers.org/hco/7/GRCh38#96964441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6820066-C-A

96964489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6820121-T-G

96964493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6820125-G-A

http://identifiers.org/hco/7/GRCh38#96964603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6820243-C-A

96964693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6820325-A-T

96964712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6820346-T-C

96964713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6820347-T-G

96964717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6820351-T-C

96964795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6820427-G-T

http://identifiers.org/hco/7/GRCh38#96964802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6820434-C-A

96965005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6820640-C-T

96965092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6820732-G-T

http://identifiers.org/hco/7/GRCh38#96965123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6820756-C-A

http://identifiers.org/hco/7/GRCh38#96965154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6820788-C-A

96965200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6820839-G-T

http://identifiers.org/hco/7/GRCh38#96965284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6820923-C-A

96965484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6821124-T-C

96965848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6821481-T-A

96966037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6822161-A-G

96966045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6822170-T-C

96966294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6822379-T-C

96966412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6822496-A-T

96966673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6822690-G-A

96966684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6822701-T-C

96966738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6822752-T-C

96966760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6822774-C-T

http://identifiers.org/hco/7/GRCh38#96967284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6822972-C-A

96967395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6823080-G-T

96967443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6823103-G-A

96967565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6823201-G-A

96967819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6823466-T-C

http://identifiers.org/hco/7/GRCh38#96967997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6823642-C-A

96968018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6823663-G-A

96968026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6823671-G-T

http://identifiers.org/hco/7/GRCh38#96968110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6823749-C-A

96968197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6823789-A-G

96968492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6824038-A-G

96968497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6824043-G-A

96968497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6824043-G-T

96968663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6824158-G-T

http://identifiers.org/hco/7/GRCh38#96968702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6824202-C-A

96968756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6824254-T-C

96968798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6824284-G-A

http://identifiers.org/hco/7/GRCh38#96968838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6824322-A-C

96968838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6824322-A-G

96968883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6824367-G-T

96969066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: non coding transcript exon variant
orthologous variants: 6824528-A-G

96969284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824732-G-A

96969608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6825015-A-T

http://identifiers.org/hco/7/GRCh38#96969621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6825028-C-A

96969718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6825128-T-A

96969718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6825128-T-C

96969959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6825340-T-C

96969991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6825376-G-T

96970079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6825944-C-T

96970097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6825962-T-C

http://identifiers.org/hco/7/GRCh38#96970235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6826094-C-A

96970235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826094-C-G

96970303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826187-C-T

http://identifiers.org/hco/7/GRCh38#96970448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6826300-A-C

96970600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826440-C-G

96970849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826652-C-T

http://identifiers.org/hco/7/GRCh38#96970870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6826672-C-A

96971334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6827410-A-G

96972027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6828489-T-C

96972218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6828685-T-C

96972468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6828881-T-A

http://identifiers.org/hco/7/GRCh38#96972876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6829470-C-A

96972876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6829470-C-G

96972990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6829542-G-A

96973138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6829658-A-G

96973169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6829669-G-C

96973783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6830213-G-T

96973821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6830251-G-A

96974513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6830950-G-A

96974587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6831020-T-G

96974590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6831023-A-G

96974645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6831071-G-A

96974987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832607-T-A

96975039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832657-A-G

96975082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832700-G-A

http://identifiers.org/hco/7/GRCh38#96975092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6832710-A-C

96975386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832995-G-T

96975630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6833353-G-A

http://identifiers.org/hco/7/GRCh38#96975684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6833427-A-C

96975684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6833427-A-G

96975703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6833449-C-T

96975709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6833455-G-A

96975709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6833455-G-C

96976041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6833827-T-C

96976053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6833839-C-T

96976246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6834005-G-A

96976507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6834477-A-G

96976573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6834542-G-C

96977042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6834996-C-T

96977092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835046-G-A

96977375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835338-A-G

96977520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835464-T-C

96977873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835780-A-G

96977962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835872-T-C

96977991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835899-G-T

96978072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835940-T-C

http://identifiers.org/hco/7/GRCh38#96978139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6835997-A-C

96978139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835997-A-G

96978267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6836096-G-A

96978267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6836096-G-T

96978315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6836143-T-C

96978348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6836168-A-G

96978369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6836192-C-T

96978437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6836261-A-G

96978557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6836391-A-T

96978603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6836436-A-G

96978625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6836458-T-C

96978794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6836610-G-A

96978877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6836701-T-C

96978885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6836709-T-G

http://identifiers.org/hco/7/GRCh38#96978914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6836738-C-A

96978914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6836738-C-T

96978944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6836768-G-T

96979177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6836957-T-C

96979178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6836958-G-T

http://identifiers.org/hco/7/GRCh38#96979204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6836982-A-C

96979663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6837253-C-G

http://identifiers.org/hco/7/GRCh38#96979667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6837257-C-A

96979667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6837257-C-G

http://identifiers.org/hco/7/GRCh38#96979669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6837259-C-A

96979669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6837259-C-G

96979669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6837259-C-T

96979682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6837273-A-T

96980118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6837704-G-T

96980349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6837937-T-A

96980349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6837937-T-C

96980463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6838046-C-G

96980482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6838065-T-C

96980572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6838153-G-A

96981102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6838613-T-C

96982156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6841104-G-A

96982669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6841255-G-A

96982706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6841288-G-A

96983144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6841713-G-T

96983146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6841715-A-G

96983352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6841904-C-G

http://identifiers.org/hco/7/GRCh38#96983465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6842016-A-C

96984452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6842866-G-C

http://identifiers.org/hco/7/GRCh38#96985478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6843678-C-A

96985509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6843706-G-A

96985693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6843881-A-G

96985742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6843930-A-G

96985749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6843937-T-C

96986141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6844545-G-C

96986710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6845140-G-A

96986710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6845140-G-T

96986748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6845177-G-T

96986923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6845349-A-G

96987099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6845502-C-T

96987344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6845745-A-G

96987657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6846231-G-A

96987782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6846373-C-T

http://identifiers.org/hco/7/GRCh38#96987906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6846493-C-A

96987994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6846582-C-T

96988699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6847410-A-T

http://identifiers.org/hco/7/GRCh38#96989261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#6847966-C-A

96989267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6847972-T-C

96989326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6848019-A-G

96989743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6848323-G-A

96989869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6848445-G-A

96990080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6848631-A-G

96990871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6849028-A-G

96991346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6849494-A-G

96991476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6849621-G-C

http://identifiers.org/hco/7/GRCh38#96991864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6850003-C-A

96991916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6850055-G-A

96992275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6850431-G-A

96992275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6850431-G-C

96992380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6850511-T-C

96992417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6850558-A-G

96992513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6850635-T-C

96992516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6850638-C-T

96992793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6850875-G-A

96992826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6850881-C-T

96992866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6850920-A-T

96992911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6850978-G-C

96992957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6851024-C-T

96993019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6851076-A-T

http://identifiers.org/hco/7/GRCh38#96993075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6851132-A-C

http://identifiers.org/hco/7/GRCh38#96993290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6851325-C-A

96993966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6851925-G-A

96994545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6852477-C-T

96994904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6852845-A-G

96994942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6852885-G-A

96994979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6852917-T-C

96994994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6852932-T-C

96995023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6852964-T-C

http://identifiers.org/hco/7/GRCh38#96995118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6853061-A-C

http://identifiers.org/hco/7/GRCh38#96995971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6853743-A-C

http://identifiers.org/hco/7/GRCh38#96996014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6853759-C-A

96996014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6853759-C-G

96996014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6853759-C-T

96996051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6853796-T-C

96996311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6853958-G-A

96996311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6853958-G-C

http://identifiers.org/hco/7/GRCh38#96996355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6854006-A-C

96996550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6854205-T-G

http://identifiers.org/hco/7/GRCh38#96996824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6854440-C-A

96996824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6854440-C-G

96996857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6854473-G-T

96997001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6854601-T-C

96997006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6854606-T-C

96997077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6854660-A-G

96997215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6854806-G-A

96997227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6854819-A-G

96997403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6855008-G-C

http://identifiers.org/hco/7/GRCh38#96997404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6855009-C-A

96997404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6855009-C-T

96997677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6855288-G-A

96997677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6855288-G-C

96998238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6855855-G-A

96998238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6855855-G-T

96998417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6856032-G-A

96998437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6856055-A-G

96998603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6856246-G-C

96998607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6856250-G-C

96998608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6856251-G-A

96999098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6856727-C-T

96999144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6856775-C-T

96999642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6857222-C-T

96999734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6857312-G-A

http://identifiers.org/hco/7/GRCh38#96999771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6857344-C-A

96999771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6857344-C-T

96999779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6857352-G-A

96999806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6857366-T-G

97000608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6858110-G-A

97001184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6858657-C-T

97001688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6859313-G-A

http://identifiers.org/hco/7/GRCh38#97001800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6859423-A-C

97002288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6859922-A-G

97002326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6859955-T-C

97002663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6860224-C-T

97002667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6860228-G-A

97002792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6860314-A-T

97003134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6860617-A-T

97003653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6861062-G-A

97003669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6861078-G-A

97003715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6861116-G-A

97003730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6861131-T-C

97003809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6861210-G-C

http://identifiers.org/hco/7/GRCh38#97003839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6861239-C-A

97003876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6861274-G-T

97003919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6861312-T-C

97004053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6861455-T-C

97004056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6861458-C-G

97004056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6861458-C-T

97004192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6861578-G-A

97004562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6861947-T-C

97004963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6862349-A-G

97004963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6862349-A-T

97004977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6862363-A-G

97004978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6862364-T-A

97004978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6862364-T-C

97005057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6862449-C-T

http://identifiers.org/hco/7/GRCh38#97005175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6862575-A-C

97005175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6862575-A-G

97005183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6862583-G-A

97005291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6862688-G-T

97005307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6862704-G-A

97005578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6862970-G-T

97005623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6863015-T-C

97005905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6863308-G-A

97005905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6863308-G-T

97005932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6863335-T-G

97006055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6863457-G-A

97006055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6863457-G-T

97006418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6863832-G-A

97006418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6863832-G-T

http://identifiers.org/hco/7/GRCh38#97006436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6863850-C-A

97006436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6863850-C-G

97006436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6863850-C-T

http://identifiers.org/hco/7/GRCh38#97006485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6863900-C-A

97006485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6863900-C-T

97006597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864012-G-A

97006597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864012-G-C

97006597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864012-G-T

97006798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864241-G-T

97006828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864273-T-G

97006873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6864318-A-G

97006892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864342-G-T

97006898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864373-G-A

http://identifiers.org/hco/7/GRCh38#97006939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6864408-A-C

97006940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864409-G-T

97006977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864445-G-A

http://identifiers.org/hco/7/GRCh38#97006997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6864467-C-A

97006997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864467-C-T

http://identifiers.org/hco/7/GRCh38#97007231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6864684-C-A

97007274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864727-A-G

http://identifiers.org/hco/7/GRCh38#97007372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6864828-C-A

97007372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864828-C-T

97007379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864835-G-A

97007379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6864835-G-C

http://identifiers.org/hco/7/GRCh38#97007516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#6864957-A-C

97007516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6864957-A-G

97007516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6864957-A-T

97007605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865045-G-A

97007605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865045-G-C

97007605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865045-G-T

97007613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865053-G-A

97007613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865053-G-T

http://identifiers.org/hco/7/GRCh38#97007849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6865289-C-A

97007868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6865308-G-A

97007868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6865308-G-T

97007871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6865311-A-G

97007885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6865325-G-A

97007885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6865325-G-T

97007960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6865399-T-C

http://identifiers.org/hco/7/GRCh38#97007962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6865401-C-A

97007962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6865401-C-T

97008168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6865616-C-T

97008394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6865829-G-A

97008705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6866089-G-A

97008709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6866093-G-C

97008740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6866119-T-C

97009012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6866364-C-T

97009124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6866473-G-A

97009281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6866613-C-T

97009505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6866768-A-G

http://identifiers.org/hco/7/GRCh38#97009676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6866928-C-A

97009676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6866928-C-T

97009703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6866950-T-A

97009717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6866961-A-G

http://identifiers.org/hco/7/GRCh38#97009750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6866994-A-C

97009750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6866994-A-G

97009763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6867007-T-G

97009766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6867011-T-G

97009852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867097-C-T

http://identifiers.org/hco/7/GRCh38#97009903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#6867148-A-C

97009903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867148-A-G

97010148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867389-G-A

97010148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867389-G-C

http://identifiers.org/hco/7/GRCh38#97010200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#6867422-C-A

97010225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867447-A-T

97010257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867484-C-G

97010266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867493-T-G

http://identifiers.org/hco/7/GRCh38#97010325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#6867612-C-A

http://identifiers.org/hco/7/GRCh38#97010442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#6867802-C-A

97010447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867807-G-A

97010447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867807-G-C

97010447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867807-G-T

http://identifiers.org/hco/7/GRCh38#97010451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#6867811-C-A

97010451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867811-C-G

97010451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867811-C-T

97010459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867819-T-A

97010459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867819-T-C

97010567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867934-T-C

97010567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867934-T-G

http://identifiers.org/hco/7/GRCh38#97010614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#6867981-C-A

97010614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867981-C-T

97010770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6868277-G-T

97010777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6868284-A-T

97011215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6868700-C-G

97011411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6868886-C-T

97012297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6869781-G-A

97012297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6869781-G-T

97012452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6869935-A-T

97012718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6870194-G-A

http://identifiers.org/hco/7/GRCh38#97013300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6870820-A-C

97013488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6871073-C-T

97013723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6871302-A-T

97013779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6871334-G-A

http://identifiers.org/hco/7/GRCh38#97013833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6871387-C-A

97013833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6871387-C-T

http://identifiers.org/hco/7/GRCh38#97013848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#6871401-C-A

97013848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6871401-C-G

97013848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6871401-C-T