1921957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551280-T-A

1921957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551280-T-G

1922014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551224-G-A

1922014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551224-G-C

1922014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551224-G-T

http://identifiers.org/hco/1/GRCh38#1922047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155551187-C-A

1922047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551187-C-T

1922100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551087-T-C

1922101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551086-G-T

http://identifiers.org/hco/1/GRCh38#1922108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155551079-C-A

1922108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551079-C-T

1922117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551070-G-A

1922117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551070-G-T

http://identifiers.org/hco/1/GRCh38#1922124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155551049-C-A

1922124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551049-C-T

1922136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551037-G-C

1922136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551037-G-T

1922150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551023-G-A

1922150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155551023-G-T

1922186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155550968-G-A

1922186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155550968-G-T

1922230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155550922-G-A

1922230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155550922-G-T

1922253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155550899-G-T

1922262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155550890-G-T

1922269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155550884-G-T

1922322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155550825-C-T

1922330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155550817-G-T

1922336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155550811-T-C

1922336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155550811-T-G

1922339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155550808-A-T

1922490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155550696-T-A

1922490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155550696-T-C

1922563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155550675-C-T

http://identifiers.org/hco/1/GRCh38#1922719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155550521-A-C

1922719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155550521-A-G

1922719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155550521-A-T

1922728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155550512-G-A

1922730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155550510-G-T

1922816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155550423-T-C

1922817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155550422-C-T

1922828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155550411-C-G

http://identifiers.org/hco/1/GRCh38#1922833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155550397-C-A

1922833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155550397-C-T

1922940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155550333-G-A

http://identifiers.org/hco/1/GRCh38#1922984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155550297-C-A

1923082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155550199-A-G

1923110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155550171-C-T

1923179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155550091-T-C

1923324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155549949-C-G

1923324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155549949-C-T

http://identifiers.org/hco/1/GRCh38#1923333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549927-C-A

1923333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155549927-C-T

1923337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155549923-T-C

http://identifiers.org/hco/1/GRCh38#1923351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549896-C-A

1923399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549848-G-A

1923399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549848-G-C

1923399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549848-G-T

1923569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549693-G-A

1923625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155549651-T-C

1923704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549587-T-C

1923704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549587-T-G

1923711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549580-A-G

1923720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549571-G-A

http://identifiers.org/hco/1/GRCh38#1923740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549551-C-A

1923740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549551-C-G

1923740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549551-C-T

1923750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549536-T-C

1923812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549482-T-C

1923890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549404-G-A

http://identifiers.org/hco/1/GRCh38#1923971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549348-A-C

http://identifiers.org/hco/1/GRCh38#1924108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549302-C-A

1924108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549302-C-G

1924108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549302-C-T

1924110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549300-C-G

1924110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549300-C-T

http://identifiers.org/hco/1/GRCh38#1924145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549283-C-A

1924145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549283-C-G

1924145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549283-C-T

http://identifiers.org/hco/1/GRCh38#1924178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549273-C-A

1924283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549234-T-A

1924283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549234-T-C

1924283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549234-T-G

http://identifiers.org/hco/1/GRCh38#1924286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549231-C-A

1924286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549231-C-T

1924290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549227-G-A

1924290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549227-G-C

1924290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549227-G-T

http://identifiers.org/hco/1/GRCh38#1924303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549215-C-A

http://identifiers.org/hco/1/GRCh38#1924304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549210-C-A

http://identifiers.org/hco/1/GRCh38#1924359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549185-A-C

1924359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155549185-A-G

http://identifiers.org/hco/1/GRCh38#1924401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549156-C-A

1924401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155549156-C-G

1924401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155549156-C-T

1924419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155549138-G-A

1924419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549138-G-T

http://identifiers.org/hco/1/GRCh38#1924450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549107-C-A

1924450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549107-C-G

1924450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549107-C-T

http://identifiers.org/hco/1/GRCh38#1924456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549101-C-A

1924456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549101-C-G

1924456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549101-C-T

1924457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549100-G-A

1924457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155549100-G-T

1924492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549065-T-C

1924507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155549050-G-A

http://identifiers.org/hco/1/GRCh38#1924521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155549036-C-A

1924521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 155549036-C-T

1924527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155549031-A-G

1924554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155548999-G-A

1924554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155548999-G-T

http://identifiers.org/hco/1/GRCh38#1924556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155548997-C-A

1924556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155548997-C-T

http://identifiers.org/hco/1/GRCh38#1924558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155548995-C-A

http://identifiers.org/hco/1/GRCh38#1924561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155548992-C-A

1924561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155548992-C-T

1925727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155548503-G-A

http://identifiers.org/hco/1/GRCh38#1925817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155548420-A-C

1925865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 155548372-G-T

1925970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155548267-G-A

1925970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155548267-G-C

1926031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155548221-G-C

1926031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155548221-G-T

http://identifiers.org/hco/1/GRCh38#1926099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155548160-C-A

1926099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155548160-C-T

1926119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155548140-G-T

1926319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155547918-C-T

http://identifiers.org/hco/1/GRCh38#1926382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155547859-C-A

1926382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547859-C-T

1926383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547858-T-C

1926384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547857-G-A

1926398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547843-G-A

1926403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547838-C-T

http://identifiers.org/hco/1/GRCh38#1926430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155547814-C-A

1926430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547814-C-G

1926430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547814-C-T

1926545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547693-C-T

1926556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547684-G-C

1926573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547667-G-A

1926594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547645-G-A

1926594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547645-G-C

1926597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547642-G-C

1926610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155547629-T-C

1926771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155547445-G-A

1926986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155547228-C-T

1927008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155547206-G-T

http://identifiers.org/hco/1/GRCh38#1927031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155547183-A-C

1927145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546999-G-A

1927145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546999-G-C

1927145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546999-G-T

http://identifiers.org/hco/1/GRCh38#1927162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155546982-C-A

1927226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546918-T-C

http://identifiers.org/hco/1/GRCh38#1927304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155546832-C-A

1927304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546832-C-T

1927349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546790-G-A

http://identifiers.org/hco/1/GRCh38#1927383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155546776-C-A

1927383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546776-C-G

1927383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546776-C-T

http://identifiers.org/hco/1/GRCh38#1927390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155546769-A-C

http://identifiers.org/hco/1/GRCh38#1927510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155546642-C-A

1927510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546642-C-T

1927538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546617-A-T

1927571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546564-G-C

1927571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546564-G-T

1927587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546538-G-T

1927611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155546515-G-A

1927611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155546515-G-T

1927743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 155546386-G-A

1927743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155546386-G-C

1927781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546346-G-A

1927781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546346-G-C

http://identifiers.org/hco/1/GRCh38#1927883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155546236-C-A

1927883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546236-C-T

1927917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155546213-G-A

http://identifiers.org/hco/1/GRCh38#1927944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155546189-A-C

1927944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155546189-A-T

1927992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155546153-G-A

1927992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155546153-G-C

1927992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155546153-G-T

http://identifiers.org/hco/1/GRCh38#1928044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155546134-C-A

1928044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155546134-C-T

1928049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155546129-G-A

1928063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155546109-A-T

http://identifiers.org/hco/1/GRCh38#1928070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155546102-C-A

1928070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155546102-C-T

1928543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155545738-C-T

1928667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155545619-G-C

1928667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155545619-G-T

http://identifiers.org/hco/1/GRCh38#1928688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155545598-C-A

1928688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155545598-C-T

1928751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155545490-G-A

1928751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155545490-G-T

1928761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155545475-C-G

1928761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155545475-C-T

http://identifiers.org/hco/1/GRCh38#1928826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155545406-C-A

1928826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense variant
orthologous variants: 155545406-C-G

1928874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: synonymous variant
orthologous variants: 155545358-C-G

1928874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: synonymous variant
orthologous variants: 155545358-C-T

http://identifiers.org/hco/1/GRCh38#1928939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155545288-C-A

1928939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155545288-C-G

1928939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155545288-C-T

1930045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155544655-G-A

1930045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155544655-G-T

1930099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: synonymous variant
orthologous variants: 155544601-G-A

1930099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: synonymous variant
orthologous variants: 155544601-G-T

1930103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense variant
orthologous variants: 155544597-G-A

http://identifiers.org/hco/1/GRCh38#1930342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155544358-A-C

1930342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 155544358-A-G

1930342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 155544358-A-T

1930348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155544351-A-G

http://identifiers.org/hco/1/GRCh38#1930371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155544327-C-A

1930375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155544322-G-T

http://identifiers.org/hco/1/GRCh38#1930380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155544317-C-A

1930380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155544317-C-G

1930380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155544317-C-T

1930443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155544263-A-G

1930461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155544227-G-A

1930461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155544227-G-T

1938555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540488-C-T

1938582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540449-G-A

1938674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540331-G-C

1938710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540318-G-A

1938710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540318-G-C

1938710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540318-G-T

1938717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540311-G-A

1938717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540311-G-T

http://identifiers.org/hco/1/GRCh38#1938799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155540232-C-A

1938799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540232-C-T

1938825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540224-C-T

1938826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540223-C-T

1938842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540208-C-G

1938842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155540208-C-T

1939159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539902-C-T

1939280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539791-A-T

1939445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539639-G-A

1939464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539622-G-A

1939464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539622-G-C

1939464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539622-G-T

1939468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539618-A-G

http://identifiers.org/hco/1/GRCh38#1939499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155539600-A-C

1939530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539574-G-A

1939530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539574-G-T

http://identifiers.org/hco/1/GRCh38#1939556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155539570-C-A

1939556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539570-C-G

1939556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539570-C-T

1939655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense variant
orthologous variants: 155539472-T-G

1939880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539256-C-G

1939880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539256-C-T

1939988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155539049-G-A

1940040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155538940-T-C

1940096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155538820-G-A

1940096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155538820-G-T

1940155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155538767-C-T

1940265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155538605-C-T

1940436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155538439-C-T

1940438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155538437-C-G

1941958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536329-G-A

1941958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536329-G-T

http://identifiers.org/hco/1/GRCh38#1942007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155536284-C-A

1942049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense variant
orthologous variants: 155536240-A-G

http://identifiers.org/hco/1/GRCh38#1942109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155536180-C-A

1942180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536125-G-A

1942192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536113-A-G

1942222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536094-T-A

1942222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536094-T-C

1942222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536094-T-G

1942226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536090-G-A

1942226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536090-G-T

1942230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536086-T-C

http://identifiers.org/hco/1/GRCh38#1942246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155536070-A-C

1942246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536070-A-G

1942246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536070-A-T

http://identifiers.org/hco/1/GRCh38#1942276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155536040-A-C

1942276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536040-A-G

1942297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536017-T-C

http://identifiers.org/hco/1/GRCh38#1942301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155536013-C-A

1942301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155536013-C-T

http://identifiers.org/hco/1/GRCh38#1944546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155531003-C-A

1944546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155531003-C-T

1946172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155526724-T-C

1946221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155526675-G-A

1946221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155526675-G-T

http://identifiers.org/hco/1/GRCh38#1946251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155526643-C-A

1946251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron variant
orthologous variants: 155526643-C-T

http://identifiers.org/hco/1/GRCh38#1946317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155526594-C-A

1946317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 155526594-C-T

1946328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: stop gained
orthologous variants: 155526583-G-A

http://identifiers.org/hco/1/GRCh38#1946459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155526451-A-C

1946473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155526434-G-A

1946473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155526434-G-C

1946473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155526434-G-T

http://identifiers.org/hco/1/GRCh38#1946546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155526359-C-A

1946557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155526348-G-T

1946578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155526332-G-A

1946578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155526332-G-T

1946587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155526323-C-T

1946619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155526292-G-A

http://identifiers.org/hco/1/GRCh38#1946843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155525908-C-A

1946843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155525908-C-G

1946857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155525893-T-C

1946860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155525890-G-A

1946860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155525890-G-T

1946861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155525889-G-A

1946861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155525889-G-T

1947012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155525751-T-A

1947012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155525751-T-C

1947068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155525680-G-A

1955762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155522709-G-A

1955837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155522634-G-A

http://identifiers.org/hco/1/GRCh38#1955970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155522531-C-A

1955999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155522507-T-A

1956444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155521749-T-A

1956469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155521739-T-C

1956687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155521267-G-A

1956723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155521231-C-G

1956723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155521231-C-T

1956729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155521225-G-A

1956806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155521148-A-G

1956815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155521139-C-T

1956821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155521101-G-A

1956821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155521101-G-C

1956845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155520983-T-C

1956857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155520971-G-A

1956857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155520971-G-T

1956875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155520946-G-A

1956875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155520946-G-T

1956877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155520944-C-T

1956942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155520885-T-C

1956970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155520857-C-T

1957288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155520591-A-G

1958133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155519825-G-A

http://identifiers.org/hco/1/GRCh38#1958160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155519805-A-C

1958298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155519671-G-A

1958349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155519620-C-T

1958576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155519341-A-G

1958937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155518987-T-G

http://identifiers.org/hco/1/GRCh38#1959225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155518731-A-C

1959225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155518731-A-G

1959225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155518731-A-T

http://identifiers.org/hco/1/GRCh38#1959959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#155518518-C-A

1960100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155518384-A-G

1960100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155518384-A-T

1960116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155518368-G-A

1960116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155518368-G-T

1960577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155517684-G-A

http://identifiers.org/hco/1/GRCh38#1960705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155517505-C-A

1960714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155517496-C-T

1960823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155517301-T-C

1960922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155517184-T-C

1960922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155517184-T-G

1961162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516929-C-T

1961169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516922-G-A

1961172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516919-G-A

1961239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516844-G-C

http://identifiers.org/hco/1/GRCh38#1961282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155516802-A-C

1961390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516588-G-A

http://identifiers.org/hco/1/GRCh38#1961450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155516449-C-A

1961457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516441-A-G

1961567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516212-G-A

1961567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516212-G-C

1961590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516189-C-T

1961591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516188-G-A

1961626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516156-A-G

1961656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516145-A-G

http://identifiers.org/hco/1/GRCh38#1961673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155516129-C-A

1961682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516120-C-T

1961811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155516000-A-G

1961815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155515996-C-T

1961894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155515916-G-A

1961906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155515906-G-A

1961906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155515906-G-C

1961931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155515882-C-T

1963744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155514453-C-T

1963933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155514271-A-G

1963967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155514257-G-A

1963967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155514257-G-C

1963967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155514257-G-T

1964824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155513793-G-A

1964846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155513781-G-A

1964846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155513781-G-C

1964846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155513781-G-T

1964879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155513762-C-T

1964903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155513738-C-T

1964913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155513728-C-T

1965076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155513565-G-C

1965076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155513565-G-T

1965518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155512965-G-A

1965951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155512629-C-T

http://identifiers.org/hco/1/GRCh38#1965995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155512583-A-C

http://identifiers.org/hco/1/GRCh38#1966364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155511890-C-A

1966364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155511890-C-T

1966379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155511875-G-A

1966379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155511875-G-T

1966404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155511856-A-G

1966532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155511719-G-A

1966532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155511719-G-T

http://identifiers.org/hco/1/GRCh38#1966561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155511691-C-A

1966561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155511691-C-T

1968573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155510711-T-A

1968573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155510711-T-C

http://identifiers.org/hco/1/GRCh38#1968592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155510690-C-A

1968613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155510669-T-A

1968613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155510669-T-C

http://identifiers.org/hco/1/GRCh38#1968716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155510572-C-A

1968735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155510553-G-A

1968735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155510553-G-T

http://identifiers.org/hco/1/GRCh38#1968786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155510499-C-A

1968786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155510499-C-T

1968787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155510498-G-A

1968787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155510498-G-C

1968787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155510498-G-T

1968962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155510377-G-A

1968962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155510377-G-T

1969104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155510238-A-G

http://identifiers.org/hco/1/GRCh38#1969133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155510213-C-A

1969133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155510213-C-T

1969141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155510205-T-C

1969205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155510140-G-A

1969832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155509799-A-G

http://identifiers.org/hco/1/GRCh38#1969854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155509777-A-C

1969872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155509759-G-A

http://identifiers.org/hco/1/GRCh38#1969942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155509702-C-A

1969945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155509699-A-G

1969966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155509679-A-G

1970021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155509596-G-A

1970021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155509596-G-C

1970555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155509370-A-G

http://identifiers.org/hco/1/GRCh38#1970583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155509335-C-A

http://identifiers.org/hco/1/GRCh38#1970592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155509326-C-A

1970592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155509326-C-G

1970780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 155509164-T-A

1971534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508968-G-A

http://identifiers.org/hco/1/GRCh38#1971603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155508842-C-A

1971666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508758-C-G

1971679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508745-C-G

1971679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508745-C-T

1971680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508744-G-A

1971680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508744-G-C

1971812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508627-C-T

1971905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508532-C-G

1971905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508532-C-T

http://identifiers.org/hco/1/GRCh38#1972039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155508408-A-C

1972089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155508356-A-T

1972098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508347-T-A

1972141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508298-T-C

1972143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508296-C-G

1972143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508296-C-T

1972151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508288-G-A

1972151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508288-G-C

1972151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508288-G-T

http://identifiers.org/hco/1/GRCh38#1972210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155508218-C-A

1972210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508218-C-T

1972243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508178-G-A

1972245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508176-C-T

1972304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155508121-C-T

1972894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155507880-T-C

1972894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155507880-T-G

1972967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155507794-G-A

1973254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155507641-G-A

1973263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155507631-G-C

1973370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155507534-G-A

1973377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155507527-T-C

1973900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155507279-G-A

1973900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155507279-G-C

1973900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155507279-G-T

1973950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155507259-A-G

1974023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 155507205-A-G

http://identifiers.org/hco/1/GRCh38#1974097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155507131-C-A

1974097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155507131-C-T

1985163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155507007-T-G

http://identifiers.org/hco/1/GRCh38#1985191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155506979-C-A

http://identifiers.org/hco/1/GRCh38#1985245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155506928-C-A

1985262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155506911-A-G

1985262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155506911-A-T

1985348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155506829-G-A

http://identifiers.org/hco/1/GRCh38#1985508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155506643-C-A

1985508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155506643-C-T

1985534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155506609-T-A

http://identifiers.org/hco/1/GRCh38#1985539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155506604-C-A

1985539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155506604-C-T

1985555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155506594-T-G

http://identifiers.org/hco/1/GRCh38#1985556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155506593-C-A

1985584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155506562-T-C

1986979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155504758-G-A

1986979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155504758-G-T

http://identifiers.org/hco/1/GRCh38#1987022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155504715-C-A

1987022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155504715-C-G

1987022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155504715-C-T

1987030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155504707-T-G

http://identifiers.org/hco/1/GRCh38#1987071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155504665-C-A

1987071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155504665-C-G

1987117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155504630-A-G

1987117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155504630-A-T

1987121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155504626-G-A

1987121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155504626-G-T

1987124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155504623-G-A

1987124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155504623-G-T

http://identifiers.org/hco/1/GRCh38#1987131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155504614-C-A

1987131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155504614-C-G

1987131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155504614-C-T

http://identifiers.org/hco/1/GRCh38#1987169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155504568-C-A

1987169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155504568-C-G

1987169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155504568-C-T

1987251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155504491-C-T

1988530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155503427-A-G

http://identifiers.org/hco/1/GRCh38#1988649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155503308-C-A

1988650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155503307-A-G

1988660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155503297-G-C

1988660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155503297-G-T

1988693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155503277-C-T

http://identifiers.org/hco/1/GRCh38#1988716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155503254-C-A

1988716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155503254-C-T

http://identifiers.org/hco/1/GRCh38#1988744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155503239-C-A

http://identifiers.org/hco/1/GRCh38#1988802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155503197-C-A

1988802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155503197-C-G

1988802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155503197-C-T

1988937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155503111-T-A

1988937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155503111-T-C

1988937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155503111-T-G

1988986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155503062-G-A

1988986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155503062-G-C

1988986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155503062-G-T

1990397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155500654-G-T

1990611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155500468-A-G

1990630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155500446-T-C

1990759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155500332-T-A

1990764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155500327-G-A

1990764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155500327-G-T

1990775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155500318-G-T

1990808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155500285-G-A

1990825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155500278-A-G

http://identifiers.org/hco/1/GRCh38#1990831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155500272-C-A

1990877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155500233-G-A

1990889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 155500221-C-G

1990889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 155500221-C-T

http://identifiers.org/hco/1/GRCh38#1991013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155500096-C-A

1991013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155500096-C-G

http://identifiers.org/hco/1/GRCh38#1991047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155500064-C-A

1991047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155500064-C-T

http://identifiers.org/hco/1/GRCh38#1991201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155499906-C-A

1991201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155499906-C-T

1991325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155499817-C-G

1991325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155499817-C-T

1991339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155499803-G-A

1991343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155499799-A-G

1999042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155498574-G-T

http://identifiers.org/hco/1/GRCh38#1999266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#155498378-C-A

1999266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155498378-C-T

1999267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155498377-G-A

1999510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155498142-C-T