37257874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29768868-G-A

http://identifiers.org/hco/6/GRCh38#37257903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29768897-C-A

37257903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29768897-C-T

37257910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29768905-C-G

37257995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29768990-G-T

37258038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769033-A-G

http://identifiers.org/hco/6/GRCh38#37258055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29769050-C-A

37258055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769050-C-T

37258056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769051-G-A

37258056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769051-G-T

http://identifiers.org/hco/6/GRCh38#37258120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29769103-C-A

37258120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29769103-C-T

37258222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769179-G-A

37258222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769179-G-C

37258222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769179-G-T

http://identifiers.org/hco/6/GRCh38#37258225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29769182-C-A

37258225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769182-C-G

37258225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769182-C-T

37258229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769186-G-A

37258229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769186-G-T

37258231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769188-T-C

37258231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769188-T-G

37258234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769190-G-A

37258234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769190-G-T

37258425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769401-G-A

http://identifiers.org/hco/6/GRCh38#37258790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29769741-A-C

http://identifiers.org/hco/6/GRCh38#37259213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29770169-C-A

37259780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29770996-G-A

37259828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29771039-A-G

37260148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29771360-A-G

37260255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29771414-G-A

37260336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29771488-G-T

37260369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29771523-A-G

37262664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29775492-G-T

http://identifiers.org/hco/6/GRCh38#37262774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29775597-C-A

37262901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29775706-T-C

37262909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29775714-A-G

37265154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29777308-C-T

37265847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29777844-A-T

37268677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29781936-T-C

37269028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29782248-A-G

http://identifiers.org/hco/6/GRCh38#37269488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29783330-C-A

37269488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29783330-C-T

37269729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29783529-T-A

37269729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29783529-T-C

37273464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29785167-C-G

37273498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29785201-A-G

37273632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29785334-A-G

37273868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29785583-G-A

37273899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29785618-T-C

37273989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29785714-T-C

37274224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29785930-T-C

37279167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29787256-G-A

37279167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29787256-G-T

37279170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29787259-G-A

37279170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29787259-G-T

37279278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29787340-T-C

http://identifiers.org/hco/6/GRCh38#37279317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29787379-C-A

37279317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 29787379-C-T

37279436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29787498-A-G

37279543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29787605-C-T

37279557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29787619-G-A

37279684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29787737-T-C

http://identifiers.org/hco/6/GRCh38#37279747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29787803-C-A

37279856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29787845-T-G

37280079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29788014-A-T

37280110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29788043-C-T

37280193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29788111-A-G

37280710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29788548-T-C

37280718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29788556-C-T

37280783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29788623-C-T

http://identifiers.org/hco/6/GRCh38#37281679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29789216-C-A

37282112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789500-G-A

37282112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789500-G-T

http://identifiers.org/hco/6/GRCh38#37282288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29789664-C-A

37282288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29789664-C-G

37282288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29789664-C-T

37282321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29789697-A-G

37282385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789762-G-A

37282386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789763-C-T

37282401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789784-G-T

37282457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789833-T-C

http://identifiers.org/hco/6/GRCh38#37282492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29789865-C-A

37282492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789865-C-G

37282492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789865-C-T

37282505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789878-G-A

37282505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789878-G-T

37282572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789928-G-A

37282572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789928-G-C

37282758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29790524-T-C

http://identifiers.org/hco/6/GRCh38#37282765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29790531-A-C

37282765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29790531-A-T

37282874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29790631-A-G

37283061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29790801-A-G

37283061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29790801-A-T

http://identifiers.org/hco/6/GRCh38#37283085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29790823-C-A

37283714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29791453-A-G

37284186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29791811-G-A

37284195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29791820-G-A

37284195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29791820-G-T

37284838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29792812-A-T

37287060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29794183-A-G

37287159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794255-T-A

37287159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794255-T-C

37287180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794276-G-A

37287180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794276-G-T

37287251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794334-A-G

37287482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794516-A-T

37287553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794584-C-T

37287573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794606-T-C

37288094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29795269-T-G

37289226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29795657-A-G

http://identifiers.org/hco/6/GRCh38#37289525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29795918-C-A

37289525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29795918-C-G

37289709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29796122-G-A

37290058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29796417-G-A

37290078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29796434-A-G

37290670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29797093-G-A

37290877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29797513-A-G

37290881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29797517-T-C

37290930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29797550-G-A

37291119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29797682-T-G

http://identifiers.org/hco/6/GRCh38#37291239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29797799-C-A

37291239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29797799-C-T

37291251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29797811-A-G

37291281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29797841-C-T

http://identifiers.org/hco/6/GRCh38#37291326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29797886-A-C

37291326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29797886-A-G

http://identifiers.org/hco/6/GRCh38#37291409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29797967-C-A

37291409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29797967-C-T

37291411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29797969-T-C

37291444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29797999-G-C

37291469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798027-A-G

37291470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798028-G-A

37291470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798028-G-T

http://identifiers.org/hco/6/GRCh38#37291507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29798060-C-A

37291507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798060-C-T

37291764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798256-A-G

37291850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798308-C-G

37291948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798394-G-A

http://identifiers.org/hco/6/GRCh38#37292055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29798489-C-A

37292056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798490-A-G

37297563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798866-A-G

37302116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29799700-T-C

37302117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29799701-G-A

37302164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29799750-T-C

37302255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29799837-C-T

37302280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29799862-G-A

37303761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29802818-C-T

37303945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29802959-G-A

37306168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29806186-C-T

37306720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29807030-A-G

http://identifiers.org/hco/6/GRCh38#37308991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29809486-A-C

37309047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29809544-G-T

http://identifiers.org/hco/6/GRCh38#37309290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29809771-A-C

37310731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811362-C-G

37310775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811403-T-G

37310802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811428-T-C

37310815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811437-T-C

37310825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811447-C-T

37311166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811998-G-C

37311881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29812559-C-G

37312147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29812918-A-G

37312147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29812918-A-T

37312277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29813109-C-T

37312278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29813110-C-T

37312559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29813335-T-C

37312625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813403-A-G

http://identifiers.org/hco/6/GRCh38#37312781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29813520-C-A

37312781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813520-C-T

37312793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813530-T-C

37312877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29813610-T-C

http://identifiers.org/hco/6/GRCh38#37312887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29813620-C-A

37312909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29813642-G-A

http://identifiers.org/hco/6/GRCh38#37313018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29813751-A-C

http://identifiers.org/hco/6/GRCh38#37313036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29813769-C-A

http://identifiers.org/hco/6/GRCh38#37313055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29813771-C-A

37313055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813771-C-T

37313069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813785-G-A

37313069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813785-G-T

37313072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813788-T-C

37313160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813868-A-G

37313165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813873-T-C

37313165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813873-T-G

http://identifiers.org/hco/6/GRCh38#37313698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29814076-A-C

http://identifiers.org/hco/6/GRCh38#37313974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29814969-C-A

37313974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29814969-C-G

37313984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29814979-C-T

http://identifiers.org/hco/6/GRCh38#37314023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29815010-C-A

37314023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29815010-C-T

37314025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29815012-G-A

37314025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29815012-G-T

37314135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29815098-T-C

37314148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29815106-T-A

37314468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29815406-G-A

37314541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29815488-C-T

37314726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29815639-A-T

http://identifiers.org/hco/6/GRCh38#37314793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29815707-A-C

37314793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29815707-A-G

37314989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29815898-C-T

37315066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29816849-G-A

37315066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29816849-G-C

37315066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29816849-G-T

37315106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29816888-T-G

37316606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29818738-A-G

37316641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29818771-T-A

37316641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29818771-T-C

37316655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29818785-C-T

37316892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29818976-A-G

37316936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29818999-T-C

37317025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819059-A-G

37317084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819095-A-G

37317084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819095-A-T

http://identifiers.org/hco/6/GRCh38#37317131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29819140-C-A

37317186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29819195-T-C

37317425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819235-G-A

37317425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819235-G-T

37317442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819252-G-A

37317563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819369-G-A

37317563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819369-G-C

37317569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819375-G-A

http://identifiers.org/hco/6/GRCh38#37317705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29819486-A-C

37317867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819631-G-A

http://identifiers.org/hco/6/GRCh38#37317892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29819655-A-C

37317892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819655-A-G

37317938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819690-A-G

37317953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819704-G-T

37318279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819960-A-G

37318279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29819960-A-T

37318371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29820026-G-A

37318398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29820049-G-C

http://identifiers.org/hco/6/GRCh38#37323722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29821242-C-A

37323722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29821242-C-T

37323765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29821282-A-G

37325224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29822114-T-C

37325301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29822170-G-A

37325392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29822237-C-T

37325486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29822301-A-G

http://identifiers.org/hco/6/GRCh38#37325968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#29822490-A-C

37325968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29822490-A-G

37325995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29822524-C-G

37330867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823679-C-T

37330885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823697-G-C

37330928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823745-A-G

37330928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823745-A-T

37330933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823750-T-C

37330938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823755-G-A

37330938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823755-G-T

37331148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29823922-T-C

37331148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29823922-T-G

http://identifiers.org/hco/6/GRCh38#37331256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29824021-C-A

37331256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824021-C-T

http://identifiers.org/hco/6/GRCh38#37331288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29824053-A-C

37331288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824053-A-G

37331288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824053-A-T

http://identifiers.org/hco/6/GRCh38#37331293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29824086-C-A

37331293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824086-C-T

37331323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824116-A-G

37331323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824116-A-T

http://identifiers.org/hco/6/GRCh38#37331375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29824164-C-A

37331375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824164-C-T

37331376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824165-G-A

37331376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824165-G-T

37331384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824173-G-A

37331384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824173-G-T

37331456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824243-A-G

http://identifiers.org/hco/6/GRCh38#37331481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29824267-C-A

37331481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824267-C-T

http://identifiers.org/hco/6/GRCh38#37331517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29824324-C-A

37331517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824324-C-T

http://identifiers.org/hco/6/GRCh38#37331598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29824474-C-A

37331598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824474-C-T

37331608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824484-T-C

37331611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824487-T-G

37331626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824502-C-T

37331658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824545-G-A

37331809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824819-C-T

37331929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29824936-G-T

37332110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825142-A-G

37332130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825163-G-A

http://identifiers.org/hco/6/GRCh38#37332222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29825198-C-A

37332222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825198-C-T

37332291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825249-T-C

http://identifiers.org/hco/6/GRCh38#37332296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29825254-C-A

37332351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825305-G-A

37332351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825305-G-T

http://identifiers.org/hco/6/GRCh38#37332370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29825321-A-C

37332370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825321-A-G

37332399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825328-G-T

http://identifiers.org/hco/6/GRCh38#37332467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29825391-C-A

37332480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825401-T-C

37332622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825536-T-G

37332623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825537-G-T

http://identifiers.org/hco/6/GRCh38#37332639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29825553-C-A

37332639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825553-C-T

37332681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825594-C-T

http://identifiers.org/hco/6/GRCh38#37332709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#29825632-A-C

37332709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825632-A-G

37332757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825679-A-G

37332969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21602
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29825869-C-T