http://identifiers.org/hco/16/GRCh38#20409553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119125544-C-A

20409553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 119125544-C-T

20409562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 119125553-G-T

20409567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 119125567-T-C

20409670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119125665-T-C

20409773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119125749-G-T

20409794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119125765-A-G

20409927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, undefined
orthologous variants: 119125857-G-A

20411222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119127435-G-A

20411493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: synonymous variant
orthologous variants: 119127669-A-G

20411556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: synonymous variant
orthologous variants: 119127732-G-A

20411573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: missense variant
orthologous variants: 119127749-C-G

20411573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: missense variant
orthologous variants: 119127749-C-T

20411637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: synonymous variant
orthologous variants: 119127810-G-A

http://identifiers.org/hco/16/GRCh38#20411706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119127879-C-A

20411706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 119127879-C-T

20411711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119127884-G-A

http://identifiers.org/hco/16/GRCh38#20411907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119128089-C-A

20411907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119128089-C-T

http://identifiers.org/hco/16/GRCh38#20411947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119128125-C-A

20411947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119128125-C-T

http://identifiers.org/hco/16/GRCh38#20412045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119128211-C-A

20418011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119129442-A-T

20418045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119129476-G-A

20418045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119129476-G-C

20418045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119129476-G-T

20418048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119129480-C-T

20418056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119129488-T-C

20418066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: missense variant
orthologous variants: 119129498-A-G

20418068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: missense variant
orthologous variants: 119129500-C-T

http://identifiers.org/hco/16/GRCh38#20418071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119129503-C-A

20418112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: synonymous variant
orthologous variants: 119129544-A-G

http://identifiers.org/hco/16/GRCh38#20418323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119129756-C-A

20418323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119129756-C-T

20418388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119129822-T-C

20419181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119130948-A-G

20419191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119130958-C-T

20419265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: synonymous variant
orthologous variants: 119131033-G-A

20419280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: synonymous variant
orthologous variants: 119131048-C-T

20419361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: missense variant
orthologous variants: 119131129-C-G

20419361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: synonymous variant
orthologous variants: 119131129-C-T

20419423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: missense variant
orthologous variants: 119131191-G-A

20419446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119131214-G-A

20419446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119131214-G-C

20419698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119131422-C-G

20419781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119131500-T-C

http://identifiers.org/hco/16/GRCh38#20419857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119131590-A-C

20419887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119131620-G-A

http://identifiers.org/hco/16/GRCh38#20420136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119131881-C-A

20420269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119131979-A-G

20420271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119131981-A-G

http://identifiers.org/hco/16/GRCh38#20420292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119131997-A-C

20420654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119132173-G-A

20420889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119132433-C-T

20420993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119132514-G-T

http://identifiers.org/hco/16/GRCh38#20421014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119132529-A-C

20421158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119133368-G-C

20421204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119133406-G-A

20421204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119133406-G-T

20421231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119133430-G-A

20421231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119133430-G-T

20421239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119133438-G-A

20421239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119133438-G-C

20421306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119133505-G-A

20421306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119133505-G-T

20421422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119133621-G-A

20421423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119133622-A-G

20421485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119133682-G-A

20421485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119133682-G-T

20421495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119133692-T-C

20421495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119133692-T-G

http://identifiers.org/hco/16/GRCh38#20421496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119133693-C-A

20421496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119133693-C-G

20421500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119133697-G-A

20421500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119133697-G-C

20421500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119133697-G-T

20421540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119133718-G-T

20423790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119133855-T-C

20424126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119134369-G-A

20424126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119134369-G-T

20424197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119134424-G-T

20424227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119134448-G-T

20424248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119134471-A-G

20427525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119134711-G-A

20427584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119134770-T-C

http://identifiers.org/hco/16/GRCh38#20427618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119134805-C-A

20427618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119134805-C-T

http://identifiers.org/hco/16/GRCh38#20427743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119134918-C-A

20427743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119134918-C-T

20427758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119134932-G-C

20427759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119134933-G-A

20427759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119134933-G-C

http://identifiers.org/hco/16/GRCh38#20427814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119134988-C-A

20427814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119134988-C-T

http://identifiers.org/hco/16/GRCh38#20427929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119135098-C-A

20427929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135098-C-T

20427976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135153-T-C

http://identifiers.org/hco/16/GRCh38#20427977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119135154-C-A

20427977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135154-C-T

http://identifiers.org/hco/16/GRCh38#20427983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119135160-C-A

20428009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135186-G-A

20428264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135425-G-C

20428269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135430-C-G

20428269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135430-C-T

20428313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135474-C-T

20428489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135636-G-A

20428498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135645-G-C

20428664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135794-T-G

20428686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135814-C-G

20428768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119135891-C-T

http://identifiers.org/hco/16/GRCh38#20428809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119135932-C-A

20429333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136097-C-G

20429514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136251-G-A

20429535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136270-G-T

20429543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136277-T-A

20429543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136277-T-C

http://identifiers.org/hco/16/GRCh38#20429561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119136295-A-C

20429572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136308-A-G

http://identifiers.org/hco/16/GRCh38#20429574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119136310-C-A

20429587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136323-C-T

20429604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136353-T-C

20429623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136376-G-A

20429663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136414-T-C

20429804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136555-G-A

20429875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136627-C-T

http://identifiers.org/hco/16/GRCh38#20429889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119136641-A-C

20429889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136641-A-G

http://identifiers.org/hco/16/GRCh38#20429898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119136650-C-A

http://identifiers.org/hco/16/GRCh38#20429933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119136686-A-C

20429933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136686-A-G

20429937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136690-G-A

20429937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136690-G-C

20429937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136690-G-T

20429942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119136695-C-T

http://identifiers.org/hco/16/GRCh38#20430298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119136943-C-A

20430390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119137026-A-G

20430542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119137143-A-T

http://identifiers.org/hco/16/GRCh38#20430973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119137288-C-A

20430973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119137288-C-T

20431090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119137399-A-G

http://identifiers.org/hco/16/GRCh38#20431144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119137440-C-A

20431144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119137440-C-T

20431167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119137460-G-A

20431167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119137460-G-C

20431167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119137460-G-T

20431240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119137531-C-T

20431471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119137748-G-A

20431562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119137834-G-A

20431568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119137840-G-T

20432026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119137963-G-T

20432090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119138028-T-A

20432124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119138062-G-A

20432124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119138062-G-C

http://identifiers.org/hco/16/GRCh38#20432291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119138209-C-A

20432297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119138215-G-A

20436747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119139544-C-T

20436864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119139647-G-A

20436870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119139653-T-C

http://identifiers.org/hco/16/GRCh38#20436915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119139698-C-A

20436915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119139698-C-T

http://identifiers.org/hco/16/GRCh38#20437005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119139785-A-C

20437023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119139803-G-A

20437023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119139803-G-T

20437032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119139808-G-A

20437032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119139808-G-C

20437043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119139819-G-C

20437061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119139837-G-A

20437186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 119139962-C-G

20437186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 119139962-C-T

http://identifiers.org/hco/16/GRCh38#20437202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119139971-C-A

20437202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119139971-C-T

20437230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119139997-G-A

20437230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119139997-G-C

20437230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119139997-G-T

20437244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119140010-G-A

20437433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119140199-A-G

http://identifiers.org/hco/16/GRCh38#20437440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119140206-C-A

http://identifiers.org/hco/16/GRCh38#20437442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119140207-C-A

http://identifiers.org/hco/16/GRCh38#20437443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119140208-A-C

20437443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119140208-A-G

http://identifiers.org/hco/16/GRCh38#20437496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119140271-A-C

20437496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119140271-A-G

20437529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119140310-T-C

20439063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119140493-T-C

20439066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119140496-T-C

20439191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119140630-T-C

20439254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119141019-T-C

20439283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119141048-T-G

20439300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119141065-G-C

20439606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119141353-C-T

20439630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119141376-G-A

20439654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119141400-G-A

http://identifiers.org/hco/16/GRCh38#20439761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119141504-C-A

20439761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119141504-C-T

20439780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119141523-G-A

20439780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119141523-G-T

20439788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119141528-G-A

http://identifiers.org/hco/16/GRCh38#20439847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119141587-C-A

20439847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119141587-C-T

20439942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119141682-C-T

http://identifiers.org/hco/16/GRCh38#20439956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119141694-A-C

20439965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119141703-G-A

20439995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119141728-C-G

20440057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: 119141774-T-C

http://identifiers.org/hco/16/GRCh38#20440244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119141840-C-A

http://identifiers.org/hco/16/GRCh38#20440286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119141878-A-C

http://identifiers.org/hco/16/GRCh38#20440311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119141903-C-A

20440311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119141903-C-G

20440311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119141903-C-T

20440435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119142029-C-T

20440450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: 119142045-T-A

20440483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119142078-A-T

20440495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119142090-T-C

20440600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119142184-T-C

20440633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119142217-G-A

20440633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119142217-G-T

http://identifiers.org/hco/16/GRCh38#20440634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119142218-C-A

20440634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119142218-C-T

http://identifiers.org/hco/16/GRCh38#20440658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119142242-C-A

20440658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119142242-C-T

http://identifiers.org/hco/16/GRCh38#20440717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119142289-C-A

20440737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119142308-A-G

20440764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119142335-G-A

20440764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119142335-G-T

20440840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119142402-A-G

http://identifiers.org/hco/16/GRCh38#20440913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119142476-C-A

20440923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119142486-G-A

20440976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119142532-A-T

20440985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119142541-T-A

20441274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26060
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119142698-T-C