42139868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non coding transcript exon variant
orthologous variants: 82255360-C-G

42139868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non coding transcript exon variant
orthologous variants: 82255360-C-T

42139913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non coding transcript exon variant
orthologous variants: 82255396-A-G

42140207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82273297-A-G

http://identifiers.org/hco/22/GRCh38#42140271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82273362-C-A

42140271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82273362-C-G

42140271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82273362-C-T

42140276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82273367-T-C

http://identifiers.org/hco/22/GRCh38#42140282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82273371-C-A

42140282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82273371-C-T

42140383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273472-G-A

42140384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82273473-T-C

http://identifiers.org/hco/22/GRCh38#42140423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82273512-C-A

42140423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82273512-C-T

42140437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273526-C-T

42140473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273562-G-A

42140509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273600-C-T

42140545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273643-C-T

42140551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273649-G-A

42140560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82273658-G-A

http://identifiers.org/hco/22/GRCh38#42140607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#82273705-C-A

42140607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273705-C-T

http://identifiers.org/hco/22/GRCh38#42140629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82273727-C-A

42140629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82273727-C-T

http://identifiers.org/hco/22/GRCh38#42140640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#82273738-C-A

42140640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273738-C-T

http://identifiers.org/hco/22/GRCh38#42140648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82273746-C-A

42140648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273746-C-G

42140648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273746-C-T

http://identifiers.org/hco/22/GRCh38#42140658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#82273756-C-A

42140658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273756-C-G

42140658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273756-C-T

http://identifiers.org/hco/22/GRCh38#42140664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82273762-C-A

42140664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273762-C-T

42140666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273764-C-T

http://identifiers.org/hco/22/GRCh38#42140667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82273765-C-A

42140667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273765-C-G

42140667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273765-C-T

42140675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273773-G-A

42140675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82273773-G-T

42140689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82273787-G-A

http://identifiers.org/hco/22/GRCh38#42140702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82273799-C-A

42140702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82273799-C-T

42140765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273861-C-G

42140765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273861-C-T

42140780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273872-C-T

http://identifiers.org/hco/22/GRCh38#42140806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82273897-C-A

42140806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273897-C-G

42140806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273897-C-T

42140819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273910-G-A

42140834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273922-C-G

42140834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273922-C-T

42140840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273928-C-G

42140840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273928-C-T

42140855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273930-A-G

42140855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273930-A-T

42140859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82273934-G-A

42141136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82274182-A-G

42141136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82274182-A-T

42141137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82274183-G-A

42141137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82274183-G-T

http://identifiers.org/hco/22/GRCh38#42141147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82274193-C-A

42141147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82274193-C-T

42141157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274203-G-A

42141157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274203-G-C

42141157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274203-G-T

42141160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274206-T-C

42141164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274210-G-T

http://identifiers.org/hco/22/GRCh38#42141170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82274216-C-A

42141170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274216-C-T

http://identifiers.org/hco/22/GRCh38#42141178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82274224-C-A

42141178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274224-C-G

42141178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274224-C-T

42141199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274245-G-A

42141199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274245-G-T

42141201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82274247-G-A

42141201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274247-G-T

http://identifiers.org/hco/22/GRCh38#42141207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82274253-C-A

42141207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82274253-C-T

http://identifiers.org/hco/22/GRCh38#42141208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82274254-C-A

42141208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274254-C-T

42141270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82274316-T-C

42141270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82274316-T-G

http://identifiers.org/hco/22/GRCh38#42141297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82274343-C-A

42141297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82274343-C-T

http://identifiers.org/hco/22/GRCh38#42141302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82274348-C-A

42141302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274348-C-G

42141358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274403-C-G

42141358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274403-C-T

http://identifiers.org/hco/22/GRCh38#42141385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82274428-C-A

42141385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274428-C-G

42141385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274428-C-T

42141409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274453-A-G

42141410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274454-A-G

42141419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274486-T-C

42141426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274493-G-A

42141426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274493-G-T

42141448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274516-A-G

42141515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274564-G-A

42141515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274564-G-T

42141603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274651-C-G

42141603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274651-C-T

http://identifiers.org/hco/22/GRCh38#42141613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82274661-C-A

42141613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274661-C-G

42141619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost
orthologous variants: 82274667-A-G

42141619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost
orthologous variants: 82274667-A-T

42141620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 82274668-C-G

42141620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 82274668-C-T

42141621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82274669-C-T

http://identifiers.org/hco/22/GRCh38#42141625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82274673-C-A

42141625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 82274673-C-G

42141625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 82274673-C-T

42141631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274679-G-A

42141631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274679-G-T

http://identifiers.org/hco/22/GRCh38#42141632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82274680-C-A

42141632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82274680-C-G

42141632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82274680-C-T

http://identifiers.org/hco/22/GRCh38#42141645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, stop_lost
orthologous variants: http://identifiers.org/mco/15/GRCm39#82274693-C-A

42141645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, stop_lost
orthologous variants: 82274693-C-G

42141663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82274711-G-T

42141727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82274960-T-A

42141741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82274974-G-A

42141741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82274974-G-T

42141759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82274992-G-A

42141759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82274992-G-T

42141828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275053-A-G

42141854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275079-G-A

42141854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275079-G-C

42141854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275079-G-T

42141863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275089-C-G

42141946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82275172-T-A

42141946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82275172-T-C

42142034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82275260-G-A

42142047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82275273-A-G

42142082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275508-C-T

42142086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275512-G-A

42142086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275512-G-T

42142120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275546-C-G

42142123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275549-C-G

42142123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275549-C-T

42142149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275576-T-C

42142241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275699-C-G

42142241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275699-C-T

42142242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275700-G-A

http://identifiers.org/hco/22/GRCh38#42142247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82275705-C-A

42142247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275705-C-T

42142265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275723-G-A

42142272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275730-C-T

42142274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275732-T-C

42142288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275744-C-T

42142312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275771-T-C

42142348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275800-A-T

42142362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275812-T-C

42142368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275818-G-A

42142368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275818-G-T

http://identifiers.org/hco/22/GRCh38#42142401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82275847-C-A

42142401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275847-C-T

42142421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275866-G-A

42142421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275866-G-T

http://identifiers.org/hco/22/GRCh38#42142424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82275869-C-A

42142432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275877-T-A

42142432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275877-T-G

http://identifiers.org/hco/22/GRCh38#42142441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82275886-C-A

42142441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275886-C-G

42142441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275886-C-T

42142456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82275898-C-T

42142491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82275917-G-A

42142491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82275917-G-C

42142491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82275917-G-T

42142523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82275949-G-A

42142523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82275949-G-T

http://identifiers.org/hco/22/GRCh38#42142543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82275969-C-A

42142543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82275969-C-G

42142543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82275969-C-T

http://identifiers.org/hco/22/GRCh38#42142562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82275988-A-C

42142563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82275989-G-A

42142563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82275989-G-T

42142565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82275991-G-A

42142565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82275991-G-T

42142600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82276026-A-G

42142600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82276026-A-T

http://identifiers.org/hco/22/GRCh38#42142601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276027-C-A

42142601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276027-C-G

42142601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276027-C-T

42142602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276028-G-A

42142602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276028-G-C

42142602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276028-G-T

42142605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276031-T-G

http://identifiers.org/hco/22/GRCh38#42142619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276045-C-A

42142619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276045-C-T

42142626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276052-G-A

42142626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276052-G-T

42142634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276060-G-A

42142634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276060-G-T

42142636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82276062-C-T

42142667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276103-T-A

42142667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276103-T-C

42142667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276103-T-G

http://identifiers.org/hco/22/GRCh38#42142670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276106-C-A

42142670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276106-C-T

42142708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276138-C-T

42142759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82276187-G-A

42142759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276187-G-T

http://identifiers.org/hco/22/GRCh38#42142780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276208-C-A

42142788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276216-G-C

42142807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276235-C-G

42142807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276235-C-T

42142815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276243-G-A

42142815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276243-G-C

42142815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276243-G-T

42142820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276248-G-T

42142847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82276275-C-T

42142853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82276281-G-A

42142853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82276281-G-T

42142873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276301-G-A

42142873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276301-G-T

42142875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276303-T-A

42142875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276303-T-G

42142945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276340-T-C

http://identifiers.org/hco/22/GRCh38#42142947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276342-C-A

http://identifiers.org/hco/22/GRCh38#42142971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276356-C-A

42142971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276356-C-G

42142971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276356-C-T

http://identifiers.org/hco/22/GRCh38#42142972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276357-C-A

42142982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276367-T-A

42143047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276380-G-A

42143047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276380-G-T

42143049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276382-G-A

42143049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276382-G-T

42143128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276401-G-A

42143128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276401-G-C

42143128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276401-G-T

http://identifiers.org/hco/22/GRCh38#42143168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276431-C-A

42143168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276431-C-G

42143168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276431-C-T

http://identifiers.org/hco/22/GRCh38#42143190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276458-C-A

42143190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276458-C-T

42143191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276459-T-C

http://identifiers.org/hco/22/GRCh38#42143193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276461-C-A

42143193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276461-C-G

42143193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276461-C-T

42143240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276504-G-A

42143240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276504-G-C

42143240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82276504-G-T

42143286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82276530-A-T

http://identifiers.org/hco/22/GRCh38#42143312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276539-C-A

42143312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82276539-C-T

42143359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82276559-G-A

42143359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82276559-G-C

42143359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82276559-G-T

http://identifiers.org/hco/22/GRCh38#42143437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276604-C-A

42143437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276604-C-G

42143437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276604-C-T

42143454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82276621-G-A

42143454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82276621-G-T

http://identifiers.org/hco/22/GRCh38#42143488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276655-C-A

42143488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276655-C-T

http://identifiers.org/hco/22/GRCh38#42143494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276661-C-A

42143541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82276708-G-A

42143541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82276708-G-C

42143541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82276708-G-T

http://identifiers.org/hco/22/GRCh38#42143549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82276716-C-A

42143549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276716-C-G

42143549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276716-C-T

42143573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276740-G-C

42143573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82276740-G-T

42143593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82276759-G-C

42143593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82276759-G-T

42143777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277490-A-G

http://identifiers.org/hco/22/GRCh38#42143789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82277502-C-A

42143792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277505-T-A

42143792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277505-T-C

42143792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277505-T-G

http://identifiers.org/hco/22/GRCh38#42143813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82277525-C-A

42143813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277525-C-G

42143813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277525-C-T

42143830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277546-C-G

http://identifiers.org/hco/22/GRCh38#42143831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82277547-A-C

42143849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277564-G-A

42143856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277571-G-A

42143864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277579-G-C

42143887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277602-G-A

42143887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277602-G-C

42143887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277602-G-T

42144036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277745-C-T

42144040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277749-G-T

42144050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277757-G-A

42144050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277757-G-T

http://identifiers.org/hco/22/GRCh38#42144074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82277781-C-A

42144112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277818-A-G

http://identifiers.org/hco/22/GRCh38#42144161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82277846-C-A

42144161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277846-C-G

42144172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277857-C-T

42144185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277870-T-A

42144185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277870-T-C

42144185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277870-T-G

42144207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277892-T-C

42144231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277912-G-A

42144231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277912-G-C

42144231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277912-G-T

42144235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277916-G-A

42144235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277916-G-C

42144235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82277916-G-T

42144309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82277985-T-C

42144311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82277987-G-A

42144311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82277987-G-C

42144339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82278014-C-T

42144367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82278042-T-C

42144367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82278042-T-G

42144369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82278044-G-T

42144402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82278077-G-A

42144443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82278118-G-A

42144443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82278118-G-T

http://identifiers.org/hco/22/GRCh38#42144467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82278151-C-A

42144477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82278161-A-G

42144537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82278218-G-A

42144537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82278218-G-T

http://identifiers.org/hco/22/GRCh38#42144538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82278219-C-A

42144538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82278219-C-G

42144538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82278219-C-T

http://identifiers.org/hco/22/GRCh38#42144605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82278290-C-A

42144605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2624
most severe consequence: non coding transcript exon variant
orthologous variants: 82278290-C-T