64094002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92348023-T-A

64094002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92348023-T-C

64094149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92348167-T-C

64094606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92348589-G-A

64094650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92348633-G-T

64094698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92348678-T-A

http://identifiers.org/hco/3/GRCh38#64094711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92348691-C-A

64094796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92348756-G-A

http://identifiers.org/hco/3/GRCh38#64094822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92348784-C-A

64094884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92348826-G-A

64094892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92348834-C-T

64095203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92349132-T-C

http://identifiers.org/hco/3/GRCh38#64095240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92349164-C-A

64095345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92349248-G-A

64095398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92349281-A-G

64095456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92349339-G-T

http://identifiers.org/hco/3/GRCh38#64096009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92349852-C-A

64096009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92349852-C-T

64096020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92349863-A-G

http://identifiers.org/hco/3/GRCh38#64096126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92349974-C-A

64096126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92349974-C-G

64096126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92349974-C-T

64096185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350026-T-A

64096185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350026-T-C

64096214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350053-T-A

64096231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350070-G-A

64096316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350151-T-A

64096358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350192-A-G

http://identifiers.org/hco/3/GRCh38#64096462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92350304-C-A

64096462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350304-C-T

64096484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350326-T-A

64096484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350326-T-C

http://identifiers.org/hco/3/GRCh38#64096517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92350359-C-A

64096557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350406-T-C

64096569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350419-A-G

http://identifiers.org/hco/3/GRCh38#64096661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92350510-C-A

64096661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350510-C-T

64096763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92350593-G-A

http://identifiers.org/hco/3/GRCh38#64096891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92350728-C-A

http://identifiers.org/hco/3/GRCh38#64097209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92351048-C-A

http://identifiers.org/hco/3/GRCh38#64097451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92351315-A-C

64097451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92351315-A-G

64097479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92351337-T-A

64097556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92351441-A-G

64097575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92351465-T-C

64097671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 92351563-T-C

64097749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 92351639-C-T

http://identifiers.org/hco/3/GRCh38#64097933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92351813-C-A

64097933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92351813-C-T

64097954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92351827-T-C

64098746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92352630-G-A

64098746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92352630-G-C

64098746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92352630-G-T

64098881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92352750-T-A

64098881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92352750-T-C

64098881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92352750-T-G

64098969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 92352846-C-T

64099138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92353014-G-A

64099240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92353116-T-G

64099365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92353241-G-A

64099404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92353280-G-A

64099798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 92353674-G-A

64099801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 92353677-C-T

64099834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 92353710-A-T

64099924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 92353800-G-C

http://identifiers.org/hco/3/GRCh38#64099990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92353880-C-A

64100009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92353898-G-C

64100009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92353898-G-T

http://identifiers.org/hco/3/GRCh38#64100087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92353972-C-A

64100087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92353972-C-G

64100087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92353972-C-T

64100132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92353993-T-A

64100132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92353993-T-C

64100232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354082-T-C

http://identifiers.org/hco/3/GRCh38#64100253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92354103-C-A

64100338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354162-C-G

64100355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354178-C-T

http://identifiers.org/hco/3/GRCh38#64100361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92354184-C-A

64100419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354248-T-C

64100419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354248-T-G

http://identifiers.org/hco/3/GRCh38#64100424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92354253-C-A

64100424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354253-C-T

64100457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354285-A-G

64100458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354286-G-T

64100464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354292-G-A

64100464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354292-G-T

64100504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354332-C-G

64100629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354460-G-A

64100748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354565-C-T

64100749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354566-C-T

64100760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354577-T-C

64100981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354742-G-A

64100981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354742-G-T

64100994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92354755-T-C

http://identifiers.org/hco/3/GRCh38#64101518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92355251-C-A

64101592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92355325-A-G

http://identifiers.org/hco/3/GRCh38#64101692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92355426-C-A

64101692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92355426-C-T

64101739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92355461-G-A

64101739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92355461-G-T

64103531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92356973-G-A

64103531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92356973-G-T

64103543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92356984-T-C

64103602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92357039-G-T

64103614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92357051-A-T

64104160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92357558-G-A

64104160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92357558-G-C

64104280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92357677-T-C

64104475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92357864-T-C

http://identifiers.org/hco/3/GRCh38#64104520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92357883-C-A

64104525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92357888-G-T

64104593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92357958-A-T

64104655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92358051-T-C

64104689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92358085-G-A

http://identifiers.org/hco/3/GRCh38#64104975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92358334-A-C

64105069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92358422-T-G

64105070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92358423-G-A

64105191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92358539-C-G

http://identifiers.org/hco/3/GRCh38#64105600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92358937-C-A

http://identifiers.org/hco/3/GRCh38#64105765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92359094-C-A

http://identifiers.org/hco/3/GRCh38#64105846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92359163-A-C

64105929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92359245-G-A

http://identifiers.org/hco/3/GRCh38#64105937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92359253-A-C

64105937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92359253-A-G

64106007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92359307-T-A

64106028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92359328-G-A

64106028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92359328-G-T

http://identifiers.org/hco/3/GRCh38#64106044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92359343-C-A

64106044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92359343-C-T

64106486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92359514-G-A

64106487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92359515-T-A

64106506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92359534-G-T

64106514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92359542-G-A

64106638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92359654-T-G

64106765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92359782-T-A

64106772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92359849-G-C

64107043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92360186-G-C

64107052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92360195-G-A

64107284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92360394-T-C

http://identifiers.org/hco/3/GRCh38#64107306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92360417-C-A

64107306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92360417-C-T

64107393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92360504-T-C

64107837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92360684-T-C

64107927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92360774-A-T

64107964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92360812-T-C

64108117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92361006-T-C

64108132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92361029-G-A

64108335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92361211-G-A

64108339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92361220-G-A

http://identifiers.org/hco/3/GRCh38#64108441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92361329-C-A

http://identifiers.org/hco/3/GRCh38#64108605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92361515-C-A

64110307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92361680-C-G

http://identifiers.org/hco/3/GRCh38#64110348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92361720-C-A

64110348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92361720-C-G

http://identifiers.org/hco/3/GRCh38#64110386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92361757-A-C

http://identifiers.org/hco/3/GRCh38#64110506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92361877-C-A

64110506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92361877-C-T

64110512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92361883-C-G

64111228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92363473-G-A

64111305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92363542-G-A

64111372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92363598-G-T

64111381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92363607-G-T

64111504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92363720-G-A

http://identifiers.org/hco/3/GRCh38#64111635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92363861-A-C

http://identifiers.org/hco/3/GRCh38#64112007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92364177-C-A

64112021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92364187-C-T

64112342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92364525-T-C

64112380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92364562-T-C

64120353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92364889-T-C

64120373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92364908-G-A

http://identifiers.org/hco/3/GRCh38#64120453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92364980-A-C

64120477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92365003-C-T

64120480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92365006-T-A

64120547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92365075-T-C

64120767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92365564-C-T

64120821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92365627-G-C

64120926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92365716-C-T

64120980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92365770-G-C

64121004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92365794-C-T

64121148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92365932-C-T

64121197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92365980-T-C

64121219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92366002-G-T

64121221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92366004-C-T

64121240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92366023-T-G

64121299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92366084-C-T

64121571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92366344-G-C

64121618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92366415-T-G

64121654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92366440-T-C

64121707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92366476-T-G

http://identifiers.org/hco/3/GRCh38#64121719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92366490-C-A

64121869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92366620-A-G

64122025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92366808-T-C

64122078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92366860-G-C

64122307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92367054-C-T

64122383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92367101-T-C

64122402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92367127-C-T

64122672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92367379-G-C

64122929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92367638-G-C

64122929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92367638-G-T

64122976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92367681-T-A

64123039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92367723-T-C

64125940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92368731-A-G

64126004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92368788-C-T

64126117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92368880-G-A

64126117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92368880-G-C

64126240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92369011-C-T

64126292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92369079-C-T

64126570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92369361-C-T

64127556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92369961-G-A

64127556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92369961-G-T

64127614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92370023-G-A

64127614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92370023-G-C

64127614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92370023-G-T

64127972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92370358-T-G

64128321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92370728-C-G

http://identifiers.org/hco/3/GRCh38#64128772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92371434-C-A

64128829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92371494-C-T

64129529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92371944-C-T

64131297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92372178-G-C

64131744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92372634-A-G

64131855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92372735-A-G

64131882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92372763-G-C

64132061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92372913-T-C

64132177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92372989-T-C

64132305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92373113-C-T

64132349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92373167-A-G

64132605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92373429-T-C

http://identifiers.org/hco/3/GRCh38#64132762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92373589-C-A

64132762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92373589-C-T

64132799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92373610-C-T

64132814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92373624-T-C

64132837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92373655-G-T

64132954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92373772-T-C

64133013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92373823-G-T

64133087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92373895-G-C

64133193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92374000-C-T

64133303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92374102-G-A

64133369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92374170-C-T

64133377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92374178-G-T

64133402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92374203-G-A

64133535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92374337-C-T

64133574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92374376-T-G

64133780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92374546-C-G

64134022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92374774-C-T

64134089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92374841-G-T

64134414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92375103-A-G

64134503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92375185-G-A

64134536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92375218-T-C

64134647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92375295-C-T

64134687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92375308-A-G

64134768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92375389-C-T

64136064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92375983-T-C

64136126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92376049-G-A

64136126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92376049-G-C

64136126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92376049-G-T

64136292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92376403-T-A

64136292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92376403-T-C

64136347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92376457-C-T

http://identifiers.org/hco/3/GRCh38#64136356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92376466-C-A

64136356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92376466-C-T

http://identifiers.org/hco/3/GRCh38#64136447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92376553-C-A

64136447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92376553-C-T

64136450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92376556-T-C

64136488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92376589-C-T

http://identifiers.org/hco/3/GRCh38#64136724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92377278-C-A

64136724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92377278-C-T

64136763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92377303-G-A

64136763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92377303-G-C

64137537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92377540-C-G

64137537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92377540-C-T

64137556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92377559-C-T

64137570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92377573-C-G

64137925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92377942-T-G

http://identifiers.org/hco/3/GRCh38#64138024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92378025-A-C

64138136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92378144-T-G

64138705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92379871-T-C

64138842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92380245-C-T

64138848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92380251-T-A

64138881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92380280-T-G

64138942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92380343-G-A

64138942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92380343-G-T

64138963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92380363-G-A

64138965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92380365-C-T

64139086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92380486-G-A

64139127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92380536-T-A

64139195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92380615-G-A

64139404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92380808-G-A

64139516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92380935-T-G

64139728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92381129-T-C

64139854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92381252-A-G

64140425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92381789-T-C

http://identifiers.org/hco/3/GRCh38#64140435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92381799-C-A

64140437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92381801-C-G

64140505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92381858-C-G

64140920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92382264-G-C

64140920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92382264-G-T

64141487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92382497-C-T

http://identifiers.org/hco/3/GRCh38#64141568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92382563-C-A

64141623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92382618-C-T

64141625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92382620-T-C

64141707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92382702-G-T

http://identifiers.org/hco/3/GRCh38#64141862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92382854-A-C

64141897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92382888-T-A

64141931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92382909-A-G

64141986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92382964-G-A

64141986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92382964-G-T

64142032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92383011-A-G

64142045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92383023-C-T

64142062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92383050-A-G

http://identifiers.org/hco/3/GRCh38#64142069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92383057-A-C

64142082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92383070-G-A

64142082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92383070-G-T

64142093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92383081-G-A

64142093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92383081-G-T

64143296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92385141-C-T

64143412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92385250-C-T

http://identifiers.org/hco/3/GRCh38#64143678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92385495-C-A

64143678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92385495-C-G

64143678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92385495-C-T

64143923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92385675-G-A

64143973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92385726-G-A

64143973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92385726-G-T

64143987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92385757-A-T

64144123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92385890-G-C

64144123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92385890-G-T

64144243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92385999-T-G

64146928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92387836-C-T

64147185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92388096-A-G

64147233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92388144-G-A

64147335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92388246-T-C

http://identifiers.org/hco/3/GRCh38#64147816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92388696-C-A

64147860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92388741-C-T

64147861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92388742-G-A

64147894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92388773-T-C

64147966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92388843-G-A

64148203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92389338-A-T

64148228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92389363-T-G

64148272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92389398-T-C

64148274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92389400-C-T

64148502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92389607-T-C

64148559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92389657-C-T

http://identifiers.org/hco/3/GRCh38#64148774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92389867-C-A

64148979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92390063-G-A

64148979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92390063-G-C

64149099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92390173-G-A

64149099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92390173-G-C

64149137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92390206-G-A

http://identifiers.org/hco/3/GRCh38#64149208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92390286-C-A

64149259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92390332-G-A

64149311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92390376-C-T

64149665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92390613-C-T

64149717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92390658-A-G

http://identifiers.org/hco/3/GRCh38#64149951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92390881-C-A

http://identifiers.org/hco/3/GRCh38#64150001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92390927-A-C

http://identifiers.org/hco/3/GRCh38#64150020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92390945-C-A

64150020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92390945-C-T

64150140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92391066-G-A

64150233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92391136-T-A

64150293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92391194-G-T

http://identifiers.org/hco/3/GRCh38#64150346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92391248-C-A

64150346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92391248-C-T

64150360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92391260-A-G

64150942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92391805-G-T

http://identifiers.org/hco/3/GRCh38#64151056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92391921-C-A

64151104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92391969-G-C

64151384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92392223-A-G

64151473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92392307-G-A

64151514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92392346-G-A

64151681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92392493-A-T

64151684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92392496-C-T

64151821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92392615-G-C

64151821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92392615-G-T

64151840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92392633-G-C

64152016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92392716-C-T

http://identifiers.org/hco/3/GRCh38#64152461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92393041-C-A

64152690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92393258-G-A

64152732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92393293-G-T

64152787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92393315-G-A

http://identifiers.org/hco/3/GRCh38#64152792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92393320-A-C

64152835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92393362-A-T

64153014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92393558-G-A

64153078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92393620-G-A

64153078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92393620-G-T

64153399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92393933-G-A

64153399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92393933-G-T

http://identifiers.org/hco/3/GRCh38#64153564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92394088-A-C

64153735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394193-A-G

64153906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394333-G-T

http://identifiers.org/hco/3/GRCh38#64153971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92394395-C-A

64154046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394471-G-A

64154046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394471-G-T

http://identifiers.org/hco/3/GRCh38#64154112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92394601-C-A

64154112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394601-C-T

64154184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394670-G-A

64154184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394670-G-C

64154185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394671-G-A

64154635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394811-T-C

64154669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394845-T-C

64154743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394930-T-C

64154777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394966-G-A

64154779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394968-G-A

64154779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394968-G-T

64154807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394996-G-C

64154807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92394996-G-T

64154813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92395002-C-T

64155458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92395320-T-A

64155477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92395339-G-T

64155493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92395354-G-C

64155590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92395438-G-C

64155647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92395489-T-C

64155926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92395778-T-C

64156225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92395930-T-C

64156348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92396046-G-T

64156371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92396064-T-A

64156542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92396241-G-C

64156585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92396284-C-T

64156607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92396306-T-C

64157123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92396844-G-A

64157123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92396844-G-C

64157123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92396844-G-T

64157142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92396896-C-G

64157363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 92397325-G-A

64157391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92397360-A-G

64157523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92397473-T-G

64157895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92397812-C-T

64158055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92397898-C-T

64158090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92397930-A-G

64158335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92398178-C-G

64158406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92398241-A-G

64158943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92398446-G-A

64158943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92398446-G-C

http://identifiers.org/hco/3/GRCh38#64158964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92398464-A-C

64158964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92398464-A-G

64159442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92398866-C-T

64159678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399065-A-G

64159691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399078-C-G

http://identifiers.org/hco/3/GRCh38#64159784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92399168-C-A

64159784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399168-C-G

64159784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399168-C-T

http://identifiers.org/hco/3/GRCh38#64159808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92399191-A-C

64159808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399191-A-G

64159809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399192-A-G

64159851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399253-T-C

64159851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399253-T-G

64159925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92399298-T-C

64159927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92399299-A-T

64159952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92399324-A-G

64159958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92399330-T-C

64159970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92399342-T-A

64159970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92399342-T-G

64160015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92399387-C-G

64160015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92399387-C-T

64160085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92399457-G-C

64160093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399466-C-G

64160112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399484-A-G

64160148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399519-T-C

64160185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399551-T-C

64160211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399573-A-G

64160214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399576-G-T

64160441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399782-A-G

64160478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399813-T-C

64160540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399866-G-A

http://identifiers.org/hco/3/GRCh38#64160560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92399885-C-A

64160565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399890-C-T

64160627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92399916-G-A

64160776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92400021-G-C

64160790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92400045-C-T

http://identifiers.org/hco/3/GRCh38#64160827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92400080-C-A

64160908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92400150-G-A

64161240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92400429-G-A

64161316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92400505-C-T

64161325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92400513-T-C

64161347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92400535-C-T

64161475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92400665-C-T

64161561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92400753-T-C

64161612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92400803-C-G

http://identifiers.org/hco/3/GRCh38#64161660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92400850-A-C

64162136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92401542-G-T

64162440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92401997-A-G

http://identifiers.org/hco/3/GRCh38#64162588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92402137-C-A

64162588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92402137-C-G

64162588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92402137-C-T

64162593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92402142-A-G

64162835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92402391-T-C

64162838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92402394-T-C

64163004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92402549-C-G

64163004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92402549-C-T

64163063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92402608-G-A

64163075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92402620-G-T

http://identifiers.org/hco/3/GRCh38#64163170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92402713-A-C

64163221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92402764-G-A

64163221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92402764-G-T

64163301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92402844-T-G

64163379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92402920-T-C

64163379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92402920-T-G

64163475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92403012-T-A

64163475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92403012-T-G

64163480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92403017-G-A

64163488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92403023-C-G

http://identifiers.org/hco/3/GRCh38#64163525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92403059-C-A

64163525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 92403059-C-T

64163623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92403156-G-T

64163656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92403177-T-C

64163804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 92403315-C-G

http://identifiers.org/hco/3/GRCh38#64163860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92403377-C-A

64163864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 92403381-C-T

64163890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 92403408-A-G

64164549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92404716-A-G

64164691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92404850-C-G

64164718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92404881-C-T

64164767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92404928-T-C

64164852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92405011-G-C

64165343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92405615-T-C

64165401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92405671-A-G

64165578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92405841-G-A

64165579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92405842-G-T

64165607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92405876-T-G

64165615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92405884-A-G

64165620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92405889-T-C

64165892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92406448-A-T

64165971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92406524-T-A

64166120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92406548-T-G

64166183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92406599-T-G

64166313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92406711-G-A

http://identifiers.org/hco/3/GRCh38#64166345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92406743-A-C

64166345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92406743-A-G

64166617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92406970-T-C

64166771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, undefined
orthologous variants: 92407116-T-C

64167297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92407595-T-C

64167321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92407612-G-A

64167747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92408099-A-G

64168219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92408498-T-C

64168241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92408520-G-A

64168796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92409169-T-A

64169178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92409527-T-C

64169548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92409983-C-T

http://identifiers.org/hco/3/GRCh38#64169606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92410035-A-C

http://identifiers.org/hco/3/GRCh38#64169633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92410062-C-A

http://identifiers.org/hco/3/GRCh38#64169659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92410090-A-C

64169944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92410358-G-A

64170262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92410653-A-T

64171991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92412915-C-G

64171991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92412915-C-T

64172022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92412945-T-C

64172062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92412981-C-T

64172182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92413347-A-G

64172281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92413443-C-T

64172296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92413458-C-T

64172501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92413623-T-A

64175962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92414827-C-G

64176005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92414865-T-G

64176013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92414873-A-G

64179489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92416221-G-C

64179703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92416356-T-C

64179732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, undefined
orthologous variants: 92416382-G-C

64179914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92416549-G-A

64179914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92416549-G-C

http://identifiers.org/hco/3/GRCh38#64180234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92416861-C-A

64180234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92416861-C-T

http://identifiers.org/hco/3/GRCh38#64180236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92416863-A-C

64180295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92416941-G-A

64180295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92416941-G-C

64180354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92417005-T-C

64180386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92417034-G-A

64180422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92417076-T-C

64180436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92417090-G-A

64181073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92417399-G-C

64181369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron variant
orthologous variants: 92417670-A-T

64183929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92420765-T-C

64184007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92420838-A-G

64184019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92420850-G-C

64184150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92420980-C-T

64184256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92421089-G-A

64184423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92421217-C-T

64185178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92421687-C-T

64185346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92421828-C-G

64185591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92422293-C-T

http://identifiers.org/hco/3/GRCh38#64185643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92422346-C-A

64185643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92422346-C-T

64185654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92422357-C-T

64185779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92422458-T-G

64186230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92422894-G-A

64186230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92422894-G-C

64186268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92422931-G-C

64186414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92423074-A-G

64186416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92423076-C-T

64186417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92423077-G-A

64186441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92423101-T-C

64187367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92423977-G-C

64187367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92423977-G-T

64187413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92424019-A-T

http://identifiers.org/hco/3/GRCh38#64187417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92424023-C-A

64187417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92424023-C-T

http://identifiers.org/hco/3/GRCh38#64187418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92424024-A-C

64187418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92424024-A-G

http://identifiers.org/hco/3/GRCh38#64187443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92424049-C-A

64187443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92424049-C-G

64187443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92424049-C-T

64187529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92424140-G-A

64187561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92424172-T-C

64189205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92424600-G-A

64189659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92424980-T-C

64189748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425067-T-A

64189748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425067-T-C

64189749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425068-C-G

64189761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425080-C-G

64190109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425397-C-T

64190120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425418-G-A

64190161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425452-A-G

64190162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425453-G-A

64190162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425453-G-T

http://identifiers.org/hco/3/GRCh38#64190216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92425491-C-A

64190216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425491-C-G

64190216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425491-C-T

http://identifiers.org/hco/3/GRCh38#64190232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92425506-C-A

http://identifiers.org/hco/3/GRCh38#64190259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92425532-C-A

64190284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425556-G-A

64190523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425756-G-A

64190581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92425814-T-C

64190972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92426197-G-C

64191102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92426339-G-A

64191200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92427206-T-C

64191394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92427376-T-C

64191448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92427426-A-G

64191472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92427450-T-C

64191547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92427480-C-T

64191670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92428382-G-C

64191860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92428570-G-A

64191866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92428576-C-T

64191961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92428667-G-A

http://identifiers.org/hco/3/GRCh38#64192185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92428884-C-A

64192185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92428884-C-T

64192194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92428894-C-T

64192262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92428963-C-T

64192300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92428998-G-A

64192973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92429655-T-C

64192988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92429676-T-A

64192988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92429676-T-C

http://identifiers.org/hco/3/GRCh38#64193175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92429854-A-C

64193237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92429910-C-T

64193292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92429946-A-T

http://identifiers.org/hco/3/GRCh38#64193385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92430049-A-C

64193385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92430049-A-T

64193389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92430053-T-C

64194020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92430508-G-A

64194027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92430537-A-T

http://identifiers.org/hco/3/GRCh38#64194051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92430561-C-A

64194183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92430686-G-T

64194319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92430810-G-A

http://identifiers.org/hco/3/GRCh38#64194322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92430813-C-A

64194344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92430835-G-C

64194375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92430924-T-C

http://identifiers.org/hco/3/GRCh38#64194393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92431119-C-A

64195209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92432175-A-G

64195217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92432183-T-C

http://identifiers.org/hco/3/GRCh38#64195295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92432256-C-A

64195315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92432276-T-C

64195436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92432396-C-T

64195440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92432400-G-A

64195546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92432505-C-G

64195968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92432927-C-T

64196087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92433039-G-A

64196228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92433169-T-C

64196309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92433231-G-A

http://identifiers.org/hco/3/GRCh38#64196425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92433349-C-A

64196605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92433509-C-T

64196643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92433554-C-G

64196791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92433682-G-A

64198636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92435310-T-C

64198754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435427-C-G

http://identifiers.org/hco/3/GRCh38#64198757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92435430-C-A

64198757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435430-C-T

64198769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435442-C-T

64198838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92435510-T-C

64198970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92435642-G-T

64199103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435771-G-A

64199103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435771-G-T

64199105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435773-G-A

64199105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435773-G-T

http://identifiers.org/hco/3/GRCh38#64199133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92435784-C-A

64199133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435784-C-T

64199153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435807-T-A

64199153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435807-T-C

http://identifiers.org/hco/3/GRCh38#64199184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92435841-C-A

64199184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435841-C-G

64199184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435841-C-T

http://identifiers.org/hco/3/GRCh38#64199238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92435884-C-A

64199253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435916-A-G

64199257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92435920-G-T

64199348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436022-A-G

64199377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436048-G-C

64199399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436064-T-C

64199399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436064-T-G

64199415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436083-G-A

64199415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436083-G-T

64199434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436102-A-T

64199444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436112-T-G

64199450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436118-T-A

http://identifiers.org/hco/3/GRCh38#64199455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92436123-A-C

64199490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436208-C-T

64199520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436231-G-T

http://identifiers.org/hco/3/GRCh38#64199566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92436274-C-A

64199566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436274-C-T

64199869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436815-A-G

64199871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92436817-G-T

64200109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92437034-T-C

64200207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92437129-A-T

http://identifiers.org/hco/3/GRCh38#64200253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92437174-C-A

64200410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92437331-T-C

64200442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92437364-T-C

64204871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92438075-G-C

64204963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92438167-G-A

64205013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92438216-C-T

64205178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92438476-G-A

64205288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92438596-G-A

64205325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92438634-T-C

64205387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92438696-G-C

64205684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92438857-G-A

64205684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92438857-G-T

64205800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92438966-A-G

64206173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92439322-C-T

64206764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92439920-G-A

64206831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92439987-T-C

64206889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92440047-C-T

64207236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92440094-A-G

64207489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92440326-G-A

64207505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92440342-G-A

http://identifiers.org/hco/3/GRCh38#64207584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92440527-C-A

64207841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92440766-T-C

64207842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92440767-G-A

http://identifiers.org/hco/3/GRCh38#64208133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92441028-C-A

64208133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92441028-C-G

64209651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92441378-T-C

64209742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92441499-G-T

64209750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92441507-C-T

64209751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92441508-C-G

64209810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92441562-T-C

64210477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92442192-T-A

64210743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92442427-T-C

64211063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92442714-C-T

64211088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92442735-T-A

64211748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92444226-T-C

64211750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92444228-A-G

64211763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92444236-T-C

64213445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92444952-G-A

64213445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92444952-G-C

64213552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92445054-T-A

64213553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92445055-G-C

64213663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92445170-G-A

64213663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92445170-G-C

64213756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92445268-C-T

64213767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92445276-A-T

64214147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92445649-C-T

64214677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92446153-T-G

64214805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92446262-A-T

64214847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92446304-T-C

64215120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92446490-T-C

64215124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92446494-A-G

64215124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92446494-A-T

64215126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92446496-C-T

64215525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92447003-A-T

http://identifiers.org/hco/3/GRCh38#64215738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92447432-A-C

http://identifiers.org/hco/3/GRCh38#64216081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92447768-A-C

64216081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92447768-A-T

64216218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92447891-A-G

64216499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92449116-T-A

64216636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92449249-G-A

64216636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92449249-G-C

64220180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92452125-T-A

64220180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92452125-T-C

64220511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92452436-C-G

64220610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92452814-G-A

64220625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92452829-T-C

64220631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92452835-C-T

64220684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92452888-T-A

64220723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92452924-G-A

64220861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92453569-T-G

64220928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92453620-T-C

64220960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92453649-T-C

64221420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92454065-T-C

64221525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92454340-G-A

64221584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92454405-C-T

64221666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92454479-A-G

64221687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92454499-T-C

64221761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92454568-T-C

64222211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92454967-G-A

64222211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92454967-G-T

64222339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92455118-C-T

64222371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92455150-T-C

64222508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92455581-C-T

64222552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92455619-G-A

64222588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92455665-G-A

64222601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92455694-C-T

64222825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92455908-A-G

64222842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92455925-C-T

http://identifiers.org/hco/3/GRCh38#64222906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92455990-C-A

64222906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92455990-C-T

64223095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92456152-T-C

64223159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92456202-T-C

64223337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92456356-C-T

64223643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92456674-C-T

http://identifiers.org/hco/3/GRCh38#64223647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92456678-A-C

http://identifiers.org/hco/3/GRCh38#64224000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92456974-C-A

64224000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92456974-C-T

http://identifiers.org/hco/3/GRCh38#64224027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92457001-A-C

64224199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92457143-T-C

64224592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92457543-T-G

64224727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92457663-G-A

64224762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92457694-T-C

64224822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92457745-G-A

64224822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92457745-G-T

64224926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92457821-A-G

http://identifiers.org/hco/3/GRCh38#64224929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92457824-C-A

64224929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92457824-C-T

64224954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92457849-A-G

64225134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92458033-C-T

64225161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92458060-G-C

64225161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92458060-G-T

64225244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92458137-G-A

64225244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92458137-G-T

64225434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92458319-T-G

http://identifiers.org/hco/3/GRCh38#64225540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92458433-C-A

64225615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92458526-G-A

64225615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92458526-G-T

64225961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92459007-A-G

64226075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92459101-G-A

64226161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92459189-C-G

64226198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92459225-T-C

64226261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92459287-A-G

64226319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92459336-G-A

64226326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92459349-C-T

64226677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92460065-G-A

64226853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92460341-G-A

64226981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92460477-A-T

64227169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92460671-C-T

64227335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92460825-A-G

64227354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92460844-T-C

64228332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92462185-G-A

64228552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92462343-A-T

64229296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92463048-G-C

64229560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92463261-A-G

64229583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92463280-G-A

64229661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92463347-G-C

64229954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92463653-T-G

64230158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92463887-C-T

64230252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92463978-C-T

64230705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92464429-A-G

64230813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92464686-T-A

64230813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92464686-T-C

64230813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92464686-T-G

64230832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92464704-C-T

64231211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92465077-T-C

64231368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92465238-G-C

64231633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92466163-G-A

64231701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92466233-T-C

64232191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92466680-A-T

64232517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92467286-T-C

64232606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92467354-C-T

64233039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92467839-T-C

64233254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92468042-C-G

64237857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92475663-T-G

64237934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92475732-C-G

64238638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476086-A-G

64239111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476535-C-T

64239137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476561-C-T

64239241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476662-G-A

64239241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476662-G-C

64239252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476672-G-A

64239252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476672-G-C

http://identifiers.org/hco/3/GRCh38#64239326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92476740-C-A

64239388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476792-T-G

http://identifiers.org/hco/3/GRCh38#64239399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92476803-A-C

64239699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92477033-A-G

64239759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92477048-G-A

64240402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92477441-G-A

http://identifiers.org/hco/3/GRCh38#64240648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92477563-C-A

64241007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92477855-C-G

64241007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92477855-C-T

64241864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92479975-T-G

64242204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92480686-T-C

64242219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92480701-A-G

http://identifiers.org/hco/3/GRCh38#64242278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92480759-A-C

http://identifiers.org/hco/3/GRCh38#64242794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92481190-C-A

64242794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92481190-C-T

64243138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92481517-C-T

64243179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92481550-C-T

64243198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92481568-G-A

http://identifiers.org/hco/3/GRCh38#64243374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92481897-C-A

64243374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92481897-C-T

64243395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92481917-T-C

http://identifiers.org/hco/3/GRCh38#64243549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92482074-C-A

64243549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482074-C-T

64243600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482133-C-T

64243883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482901-C-G

64243885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482903-G-C

64244277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92483320-G-A

64244385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92483428-G-T

http://identifiers.org/hco/3/GRCh38#64244692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92483685-A-C

64244699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92483692-T-C

64244772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92483766-T-C

64244895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92483888-T-C

64244908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92483901-T-A

64245052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484026-G-T

http://identifiers.org/hco/3/GRCh38#64245374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92484327-C-A

64245374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484327-C-T

64245559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484721-G-A

64245587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484734-G-A

64245587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484734-G-C

64245615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484759-A-G

64245645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484789-C-G

64245698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484837-C-G

64245787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484930-C-T

64245882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92485032-G-C

64246549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92485701-G-A

64246611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92485756-A-G

http://identifiers.org/hco/3/GRCh38#64246626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92485765-A-C

64246637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92485777-G-C

64246851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92485991-A-G

64246932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92486064-G-A

64247151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92486642-C-T

64247388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92486821-T-C

64247407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92486840-T-C

64247667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92487086-C-G

64247922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92487385-C-G

64248080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92487533-G-T

64248105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92487562-T-G

64248775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488221-A-T

64248895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488307-G-A

64248952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488366-A-G

64249790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489306-T-C

64249797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489313-T-C

64249797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489313-T-G

64249963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489492-G-C

http://identifiers.org/hco/3/GRCh38#64250088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92489598-C-A

64250088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489598-C-T

64250189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489707-C-T

64250193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489711-T-C

http://identifiers.org/hco/3/GRCh38#64250250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92489768-C-A

64250268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489781-T-C

64250278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489791-T-C

64250366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489879-C-T

64250478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489965-A-T

64250778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490403-C-T

http://identifiers.org/hco/3/GRCh38#64251448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92491400-A-C

64251541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92491489-G-A

64251551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92491499-G-A

64251626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92491574-A-G

64251718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92491675-G-T

64251824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92491771-C-T

http://identifiers.org/hco/3/GRCh38#64252106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92492032-C-A

64252106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92492032-C-T

64252335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92492998-C-G

64252782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92493395-C-T

http://identifiers.org/hco/3/GRCh38#64252810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92493423-C-A

64253005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92493610-G-A

http://identifiers.org/hco/3/GRCh38#64253195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92493779-A-C

64253934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92494493-C-T

http://identifiers.org/hco/3/GRCh38#64254436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92494941-C-A

64254843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92495366-T-C

64255013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92495542-A-G

64255030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92495559-T-A

64255030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92495559-T-C

64255151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92495677-A-G

64255335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92495866-C-T

64255402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92495941-A-T

64255429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92495969-C-T

64255844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92497552-A-G

64255844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92497552-A-T

64256345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92497913-A-G

64256416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92497980-G-C

http://identifiers.org/hco/3/GRCh38#64257055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92498601-C-A

64257055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92498601-C-T

64257059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92498605-G-A

64257207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92498774-A-T

http://identifiers.org/hco/3/GRCh38#64257343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92498905-A-C

64257644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92499110-T-C

64257715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92499184-C-T

http://identifiers.org/hco/3/GRCh38#64259853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92502455-C-A

64259853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502455-C-G

64259943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502552-G-A

64259981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502597-C-T

64260248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502807-C-T

http://identifiers.org/hco/3/GRCh38#64260404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92503051-C-A

64260444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92503146-T-C

64260563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92503409-C-T

http://identifiers.org/hco/3/GRCh38#64260772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92503607-C-A

64260772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92503607-C-G

64260805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92503640-A-G

64261654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92504423-G-A

64261686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92504456-A-G

64261703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92504467-G-T

64262003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92504791-T-A

64262369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92505075-G-C

64262369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92505075-G-T

http://identifiers.org/hco/3/GRCh38#64262370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92505076-C-A

64262372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92505078-T-A

http://identifiers.org/hco/3/GRCh38#64262615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92505868-C-A

64262624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92505877-T-A

64262624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92505877-T-C

64262712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92505959-T-C

64263054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506255-A-G

64263194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506401-C-T

64263280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506466-G-A

64263284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506470-G-T

64263297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506482-C-T

64263552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506598-G-A

64263826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506854-A-T

64263864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506888-T-C

64263980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507002-T-C

64264312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507223-A-G

http://identifiers.org/hco/3/GRCh38#64264544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92507438-A-C

64265274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508506-C-G

http://identifiers.org/hco/3/GRCh38#64265335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92508558-C-A

64265753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508978-T-C

64265844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92509070-C-G

64265851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92509077-T-G

64266078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92509448-G-C

64266203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92509690-A-G

64266749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92510397-G-A

64266749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92510397-G-T

64267248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92510934-T-A

64267248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92510934-T-C

64267276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92510965-C-T

64267495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511174-A-G

64267855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511549-C-T

64267886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511582-G-A

64267886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511582-G-C

64267886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511582-G-T

http://identifiers.org/hco/3/GRCh38#64267921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92511616-C-A

64267921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92511616-C-T

64267998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92511695-G-A

64267998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92511695-G-T

http://identifiers.org/hco/3/GRCh38#64268021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92511712-C-A

64268021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92511712-C-T

http://identifiers.org/hco/3/GRCh38#64268024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92511715-C-A

64268024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92511715-C-T

64268103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92511794-C-T

64268155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92511844-G-A

64268155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92511844-G-T

64268187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511868-C-G

64268211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511892-C-G

64268266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511948-C-T

64268283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511965-A-G

64268484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92512151-C-T

64268590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92512223-T-C

64268716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92512332-C-T

64269189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92512535-T-C

http://identifiers.org/hco/3/GRCh38#64269224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92512570-A-C

64269285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92512637-T-C

64269424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92512770-C-T

64269429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92512775-C-T

64269879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92513417-C-T

64269949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92513523-T-G

64270059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92513676-G-A

64270059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92513676-G-T

64270094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92513711-C-T

64270097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92513714-T-C

64270124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92513764-G-A

http://identifiers.org/hco/3/GRCh38#64270128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92513768-C-A

http://identifiers.org/hco/3/GRCh38#64270424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92513988-C-A

http://identifiers.org/hco/3/GRCh38#64271403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92514678-C-A

64271534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92514779-T-C

http://identifiers.org/hco/3/GRCh38#64271723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92514902-C-A

64271723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92514902-C-T

64271816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92514978-A-G

64271816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92514978-A-T

64272121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92515307-C-G

64272680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92515848-G-A

64272800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92515964-T-C

64272864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516024-A-G

64272864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516024-A-T

64272918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516079-A-T

64273086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516248-A-G

64273366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516532-C-G

64273530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516741-C-T

64273786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516985-G-A

64275408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92518038-A-G

64275560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92518138-G-A

64275962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92518681-C-G

64275987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92518706-T-G

64276146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92518909-C-T

64276199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92518972-T-C

64278882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92519129-G-A

64279164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92519389-G-A

64279164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92519389-G-C

64279429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92519711-G-T

64280592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92520756-C-G

64280781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92520931-T-C

64280854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92521008-A-G

64280942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92521084-T-C

64281291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92521343-G-A

64281402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92521449-A-G

http://identifiers.org/hco/3/GRCh38#64281423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92521467-C-A

64281611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92521646-G-A

64281620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92521655-G-C

http://identifiers.org/hco/3/GRCh38#64281721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92521758-A-C

64282904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92522897-C-T

64283555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92523841-T-A

64283610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92523891-G-C

64283774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92524063-G-T

64283897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92524206-C-T

64283926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92524236-T-C

64284021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92524316-T-C

64284976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92524919-C-T

64285241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92525118-G-T

64285689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92525578-A-G

http://identifiers.org/hco/3/GRCh38#64285916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92525873-C-A

64286359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92526310-G-A

64286666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92526619-C-G

64286884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92526846-T-C

64289217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92527594-A-G

64289612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92527963-G-A

64289612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92527963-G-C

64289712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92528021-A-T

64290238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92528577-T-C

64294036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533853-T-G

64294103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533916-C-G

64294299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92534200-A-G

64294411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92534279-C-T

64294723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92534578-C-T

64294724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92534579-A-G

64294746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92534601-A-T

64295152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92535015-C-T

http://identifiers.org/hco/3/GRCh38#64295190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92535053-A-C

64296559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92537357-T-G

64296627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92537418-A-T

64296670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92537461-T-A

64296744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92537535-T-G

64296806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92537591-A-T

64296925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92537693-T-A

64296925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92537693-T-C

64297057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92537841-G-A

64297357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92538092-A-G

64297629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92538326-T-C

64297656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92538351-A-G

64301973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92544114-T-G

64301976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92544117-T-G

64302471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92544233-G-A

64302539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92544283-A-G

64302725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92544489-C-T

64302764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92544528-G-A

http://identifiers.org/hco/3/GRCh38#64302944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92544709-C-A

64302967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92544759-C-G

64303047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92544834-C-G

64303074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92544860-T-C

64303079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92544865-A-G

64304885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92546166-C-T

64305183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92546473-C-T

64305453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92546729-C-T

http://identifiers.org/hco/3/GRCh38#64305676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92546938-C-A

64305676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92546938-C-G

64305820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92547071-G-C

64305878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92547125-G-A

http://identifiers.org/hco/3/GRCh38#64306156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92547404-A-C

http://identifiers.org/hco/3/GRCh38#64306320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92547570-C-A

64306355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92547605-T-A

64306355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92547605-T-C

64306451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92547696-T-G

http://identifiers.org/hco/3/GRCh38#64306472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92547892-C-A

64306474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92547894-C-T

64306490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92547910-A-G

64306650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92548219-T-C

64306784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92548367-G-C

64306823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92548396-A-G

64306874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92548458-A-T

64307110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92548710-C-T

64307198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92548798-G-C

64307213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92548813-A-G

64307677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92549336-G-A

64307786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92549427-C-G

64311235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92551792-C-T

64311371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92551912-C-T

64311421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92551956-T-C

64311449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92551983-T-C

64311720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92552256-C-T

64312154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92552674-T-C

64312277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92552798-T-C

64312378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92552880-A-G

64314335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92555670-C-T

64314450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92555779-C-T

64314478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92555807-C-G

64317740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92557041-A-G

64318624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92558649-T-C

64318838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92558857-C-T

64318865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92558882-C-T

64319202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92559140-A-G

64319223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92559160-C-T

http://identifiers.org/hco/3/GRCh38#64319333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92559270-C-A

64319339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92559276-G-A

64319425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92559357-G-C

64319558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92559465-G-C

64319630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92559523-T-C

64319776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92559658-T-C

64319776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92559658-T-G

64319856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92559750-T-C

64319984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92559860-T-C

64320825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92560335-G-T

64321278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92560530-G-C

64321356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92560605-A-T

64321606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92560875-G-A

http://identifiers.org/hco/3/GRCh38#64321662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92560951-C-A

64321662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92560951-C-T

64323268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92563168-A-G

64323511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92563424-T-C

64323511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92563424-T-G

64323527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92563436-T-A

64323685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92563585-G-A

64327294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92566598-C-T

64327340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92566644-C-T

64327378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92566677-G-A

64327397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92566697-G-C

64327581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92566848-C-T

64327627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92566895-C-T

64327635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92566903-G-T

64328231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92566914-G-A

64328399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92567035-C-G

64328973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92567876-G-C

64329332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92568192-T-C

64330011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92569478-A-T

64330124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92569587-T-A

64330124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92569587-T-C

64330140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92569603-C-T

64330198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92569661-G-A

64330280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92569735-C-T

64330291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92569746-T-C

64330306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92569761-A-G

64330359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92569811-A-G

64330393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92570472-T-C

64330482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92570557-G-T

64330596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92570635-G-T

64331444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92571301-A-T

64331488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92571345-G-C

64331760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92572278-G-A

64331769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92572287-A-G

64331827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92572339-C-T

64331846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92572358-C-T

64332303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573155-G-A

64332307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573159-T-C

64332309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573161-A-G

64332692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573536-G-C

64332708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573551-T-A

64332763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573603-T-A

64332763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573603-T-C

64332802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573641-T-C

64332890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573709-G-C

64332930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573749-G-A

64332930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573749-G-C

64333069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573854-A-G

64333090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573875-C-T

64333154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573946-T-C

64333183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92573975-A-T

64333249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92574030-C-T

64333490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92574200-A-G

64333504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92574211-G-C

64333535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92574256-C-G

64333596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92574285-G-A

64333605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92574294-A-G

64333972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92574674-G-A

64334018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92574710-A-G

64334026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92574718-A-T

http://identifiers.org/hco/3/GRCh38#64334028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92574720-C-A

64334028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92574720-C-T

64334209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92574856-A-G

64334471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92575116-A-G

64334506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92575135-A-G

64334582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92575212-G-A

64334909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92575650-T-C

64339925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92580089-G-A

64340012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92580176-T-C

64340021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92580185-C-T

64340295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92580435-G-A

64340295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92580435-G-T

64340369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92580505-T-C

64340714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92580845-T-C

64340830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92581685-G-A

64341766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92582644-C-T

64342027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92582907-A-G

64342709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583535-T-C

64342754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92583580-G-A

64342775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583601-C-T

64342808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92583643-T-A

64342808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92583643-T-G

64342817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92583653-A-G

64343640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92584994-T-C

64343687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585041-C-T

64343708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585062-A-G

64343853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585207-T-C

64343864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585216-C-T

64343916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585268-A-G

64344423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585749-C-T

http://identifiers.org/hco/3/GRCh38#64344476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92585796-C-A

64344483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585804-C-T

64344529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585846-A-G

64344655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585967-C-T

64344676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92585988-G-A

64344676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92585988-G-T

64344808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92586125-G-A

64344934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92586285-G-A

64344934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92586285-G-C

64344934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92586285-G-T

64345043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92586367-C-T

http://identifiers.org/hco/3/GRCh38#64345304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92586604-A-C

64345635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92586934-C-T

64346042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587357-G-C

http://identifiers.org/hco/3/GRCh38#64346048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92587363-C-A

64346048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587363-C-T

64347288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587579-G-C

64347628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587921-C-T

64347878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92588161-C-T

64347895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92588178-G-C

64347895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92588178-G-T

64348022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92588284-A-G

http://identifiers.org/hco/3/GRCh38#64348182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92588453-A-C

64349398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92589349-T-C

64349658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92589597-C-T

64349955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92589876-T-C

64349969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92589894-C-T

64350545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92592011-A-T

64350630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92592083-T-C

64350801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92592247-C-T

64350807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92592253-A-T

http://identifiers.org/hco/3/GRCh38#64350891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92592302-C-A

64352554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92593252-T-C

64352676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92593371-T-G

64352687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92593380-G-C

64352783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92593471-T-C

64352836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92593525-G-A

64352875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92593560-T-C

http://identifiers.org/hco/3/GRCh38#64353359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92594172-C-A

64353359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92594172-C-T

64353975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92595023-T-C

64353990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92595037-T-C

64354008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92595055-A-G

64354211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92595213-A-G

64354275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92595280-C-T

64354344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92595335-A-T

64354363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92595361-G-A

64354445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92595437-A-G

64355578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92596941-C-T

64355602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92596965-C-G

64355725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92597086-A-G

http://identifiers.org/hco/3/GRCh38#64355797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#92597146-A-C

http://identifiers.org/hco/3/GRCh38#64355893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92597236-A-C

http://identifiers.org/hco/3/GRCh38#64355925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92597268-A-C

64355984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92597327-G-T

64356415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92597700-C-T

64356654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92597915-A-G

64356725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92597985-A-T

64358152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92599404-C-G

64358221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92599471-C-T

64359213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92600068-G-T

64359306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92600161-C-T

64359435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92600296-C-T

64359611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92600745-A-G

64359736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92600844-C-T

64359950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92601044-C-G

64359950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92601044-C-T

64360029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92601141-G-C

64360087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92601198-G-C

64360087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92601198-G-T

64360100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92601211-G-A

64360103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92601214-T-A

64360293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92601385-A-T

64360402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92601493-C-T

64360569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92601685-C-T

64360694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92607464-A-G

64360694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92607464-A-T

64360702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92607473-G-T

64361164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92607919-A-G

64361197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92607947-C-T

http://identifiers.org/hco/3/GRCh38#64361689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92608153-A-C

64361689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92608153-A-G

http://identifiers.org/hco/3/GRCh38#64361827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92608276-A-C

64361881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92608329-A-G

64361930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92608351-G-C

64361930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92608351-G-T

http://identifiers.org/hco/3/GRCh38#64361964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92608385-C-A

64362100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92608527-A-G

64362283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92608695-A-G

64362326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92609555-G-A

http://identifiers.org/hco/3/GRCh38#64362765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92610374-C-A

64363023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92610596-G-A

http://identifiers.org/hco/3/GRCh38#64363584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92611108-A-C

64363641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92611160-C-T

64363762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92611286-T-C

64363846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92611376-C-T

64370669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92612023-A-G

64370670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92612024-G-A

http://identifiers.org/hco/3/GRCh38#64370698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92612051-C-A

64370698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92612051-C-T

64370699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92612052-G-A

64370951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92612299-G-A

64371016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92612470-C-G

64371068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92612588-T-C

64371090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92612613-G-A

64371090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92612613-G-T

64371136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92612659-T-C

64371886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613046-A-G

64371934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613100-G-T

64371971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613139-G-A

http://identifiers.org/hco/3/GRCh38#64372007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92613175-C-A

64372046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613216-T-G

64372185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613351-T-C

64372275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613446-A-G

http://identifiers.org/hco/3/GRCh38#64372341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92613523-C-A

64372341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613523-C-G

64372345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613527-T-A

64372345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613527-T-C

64372396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613565-G-A

64372574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613631-C-T

64372827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613649-T-A

64372827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613649-T-C

64372870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613672-A-G

64372890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613692-C-T

http://identifiers.org/hco/3/GRCh38#64373050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92613846-A-C

64373050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613846-A-G

64373050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613846-A-T

64373141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92613933-C-T

64373704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92614339-G-A

64373853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92614498-T-A

64373988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92614614-G-C

http://identifiers.org/hco/3/GRCh38#64374146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92614750-A-C

64374150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92614756-A-G

64374324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92614933-G-A

64374332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92614941-C-T

64374470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92615075-G-C

64378619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92617970-T-C

http://identifiers.org/hco/3/GRCh38#64378761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92618107-C-A

64379080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92618777-T-C

64379315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92619036-G-A

64379321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92619042-G-T

64379555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92619276-G-A

64379612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92619357-A-G

64379612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92619357-A-T

http://identifiers.org/hco/3/GRCh38#64379767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92619496-A-C

64379971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92619624-C-T

64380028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92619667-T-C

64380030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92619669-G-A

64380692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92620336-A-T

64380949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92620524-T-C

64381130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92620698-G-C

64385203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92625345-G-A

64385230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92625364-G-C

http://identifiers.org/hco/3/GRCh38#64385386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92625542-C-A

64385386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92625542-C-G

http://identifiers.org/hco/3/GRCh38#64385524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92625686-C-A

http://identifiers.org/hco/3/GRCh38#64385639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92625807-C-A

64385639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92625807-C-T

64385860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92626016-C-T

64386266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92626512-G-A

64386428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92626675-C-T

64387438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92628052-T-C

64388494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92630796-G-A

64388629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92630928-C-T

64388990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92631481-G-A

64388990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92631481-G-T

64389773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92633163-G-A

64389773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92633163-G-T

64389985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92633364-A-G

64390133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92633491-T-C

64390359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92635619-A-G

64390374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92635633-G-A

64391317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92636083-A-G

64391468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92636229-G-C

64391476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92636237-T-A

64391506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92636297-A-T

64391568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92636369-G-A

64391663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92636468-T-A

64391663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92636468-T-C

64391688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92636491-G-A

64391688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92636491-G-T

http://identifiers.org/hco/3/GRCh38#64391851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92636608-A-C

64392361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92637116-A-G

64392535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92637274-G-A

64392559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92637293-G-A

64392608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92637342-C-G

64392760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92637486-C-G

64392805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92637533-C-G

64393057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92637784-A-G

64393057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92637784-A-T

64393209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92637945-C-G

64395078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92638329-G-A

64395517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92638783-C-G

64395598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92638862-C-T

http://identifiers.org/hco/3/GRCh38#64395968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92639198-C-A

64396263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92639442-G-A

64396428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92639582-T-C

64396700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92639851-A-T

64396721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92639863-G-A

64396893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92640033-G-A

http://identifiers.org/hco/3/GRCh38#64397036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92640102-A-C

64397100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92640172-A-T

64397296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92640359-C-T

64397426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92640469-T-A

64397872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92641355-A-G

64398117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92641738-G-A

64398163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92641784-A-G

64398301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92641928-G-A

64398314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92641941-A-G

64398314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92641941-A-T

64398367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92641980-C-G

64399551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92642799-C-T

64401815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92643357-T-A

64401842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92643384-A-G

64402029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92643752-T-A

64402096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92643866-G-A

64402181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92643930-G-A

64402181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92643930-G-T

64402347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92644088-C-T

64402755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92644161-C-G

64402819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92644227-T-A

64402889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92644295-G-A

64402889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92644295-G-C

64403317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92644766-G-A

http://identifiers.org/hco/3/GRCh38#64403384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92644827-A-C

64403410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92644852-G-T

64403714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92645134-G-A

64403714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92645134-G-C

http://identifiers.org/hco/3/GRCh38#64403727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92645147-C-A

64403729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92645149-G-A

64403871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92645285-G-A

64403871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92645285-G-C

64404329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92645615-A-T

64404517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92645765-T-G

64404747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92645986-G-C

64404899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92646143-G-A

http://identifiers.org/hco/3/GRCh38#64405082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#92646302-C-A

64405082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92646302-C-T

64405435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92646673-G-A

64405525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92646761-G-A

64405526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92646762-T-C

64405606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92646842-T-C

64405666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92646892-A-G

64405666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92646892-A-T

64405864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92647056-T-C

64405920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92647108-A-G

64405993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92647307-C-T

64405994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92647308-G-A

64406395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20340
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92647652-A-G