121918606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 123390195-G-A

http://identifiers.org/hco/12/GRCh38#121918658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123390229-C-A

121918664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: 5 prime UTR variant
orthologous variants: 123390235-G-A

121918664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: 5 prime UTR variant
orthologous variants: 123390235-G-T

121918667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: 5 prime UTR variant
orthologous variants: 123390238-G-T

http://identifiers.org/hco/12/GRCh38#121918707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#123390279-C-A

121918707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 123390279-C-G

121918707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 123390279-C-T

121918738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123390308-T-A

121918738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123390308-T-C

121918742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123390312-G-A

121918742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123390312-G-T

121918764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123390331-G-A

121918764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123390331-G-T

121919419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123391242-G-A

121919485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123391331-G-T

121919569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123391414-C-T

121922461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123393203-G-A

121922622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123393368-G-C

121923837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123394171-A-G

121923900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123394219-C-G

121923900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123394219-C-T

121923910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123394229-A-T

121923924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123394243-A-G

121923933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123394252-C-T

121924395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123394740-G-A

121924672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123394971-C-G

121924672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123394971-C-T

121924710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123395008-G-A

121924714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123395012-G-A

121924721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123395019-C-T

121924738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123395169-T-C

121924933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123395391-C-G

121924933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123395391-C-T

121928240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123398893-A-T

121928294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123398947-T-C

121928312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123398965-A-G

121931203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123399582-G-C

121931276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123399646-T-A

121931340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123399687-T-C

121931367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123399726-C-T

http://identifiers.org/hco/12/GRCh38#121931667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123399992-C-A

121931667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123399992-C-T

121931705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123400042-A-G

121931735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123400069-T-C

121931798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123400132-G-A

121931798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123400132-G-T

121931823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123400154-G-A

121931823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123400154-G-C

121931845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123400176-A-G

121931860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123400191-T-C

http://identifiers.org/hco/12/GRCh38#121931901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123400232-C-A

121931901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123400232-C-T

121932211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401293-G-T

121932240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401321-A-G

121932289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401350-G-A

121932289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401350-G-T

http://identifiers.org/hco/12/GRCh38#121932295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123401356-A-C

121932295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401356-A-T

121932296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401357-T-A

121932296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401357-T-C

121932296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401357-T-G

http://identifiers.org/hco/12/GRCh38#121932301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123401362-C-A

121932301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401362-C-T

121932316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401377-A-G

121932316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401377-A-T

http://identifiers.org/hco/12/GRCh38#121932362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123401421-C-A

121932461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401583-C-G

121932461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401583-C-T

121932480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401598-A-G

121932567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401670-T-C

121932567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401670-T-G

121932612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401712-C-T

http://identifiers.org/hco/12/GRCh38#121932635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123401735-C-A

121932661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401760-G-T

121932698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401797-G-A

121932698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401797-G-T

121932701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401800-G-C

121932725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401824-A-T

121932841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401904-G-A

121932864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401924-G-T

121932894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401949-T-C

121932924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123401978-A-G

http://identifiers.org/hco/12/GRCh38#121933003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123402030-C-A

121933003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123402030-C-T

121933051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123402062-G-A

121933051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123402062-G-C

121933062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123402073-A-G

121933208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123402212-G-T

121933269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123402269-T-C

http://identifiers.org/hco/12/GRCh38#121933348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123402328-C-A

121933348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123402328-C-T

121933498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123402366-G-T

http://identifiers.org/hco/12/GRCh38#121933576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123402388-A-C

121933576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123402388-A-G

121933576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123402388-A-T

121933577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123402389-G-A

121933577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123402389-G-T

121933926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123402576-G-A

121933927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123402577-T-A

121933938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123402587-G-A

121934120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123402735-G-T

http://identifiers.org/hco/12/GRCh38#121934130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123402745-C-A

121934130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123402745-C-T

http://identifiers.org/hco/12/GRCh38#121934225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123402832-C-A

121934225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123402832-C-G

121934225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123402832-C-T

http://identifiers.org/hco/12/GRCh38#121934233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123402840-C-A

121934233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123402840-C-T

121934288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123402895-C-G

121934413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123402996-T-C

121934414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123402997-G-A

http://identifiers.org/hco/12/GRCh38#121934532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123403111-C-A

121939024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123406942-G-A

121939141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123407066-G-A

121939274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123407194-A-G

121940498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123409089-C-G

121940498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123409089-C-T

121940514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123409105-G-C

121940514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123409105-G-T

121940523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123409114-A-G

121940662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123409196-C-G

121940662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123409196-C-T

121940704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123409235-A-G

121940936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123409444-T-C

121942390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123411688-T-C

121942484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411755-G-A

121942484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411755-G-T

121942576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123411857-T-C

121942666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411942-G-C

121942666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411942-G-T

http://identifiers.org/hco/12/GRCh38#121942686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123411962-C-A

121942686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411962-C-T

http://identifiers.org/hco/12/GRCh38#121942691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123411965-C-A

121942691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411965-C-T

121942694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411968-T-C

121942695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411969-G-T

121942700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411974-G-A

121942700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411974-G-C

121942715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411989-G-T

121942813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123412125-T-G

121942984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123412337-A-G

http://identifiers.org/hco/12/GRCh38#121943005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123412358-A-C

121944048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123412712-C-G

121944048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123412712-C-T

121944062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123412726-C-G

121944077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123412741-C-T

121944184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123412830-G-A

121944185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123412831-G-T

http://identifiers.org/hco/12/GRCh38#121944204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123412842-C-A

http://identifiers.org/hco/12/GRCh38#121944213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123412851-C-A

http://identifiers.org/hco/12/GRCh38#121944226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123412864-C-A

121944226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123412864-C-G

http://identifiers.org/hco/12/GRCh38#121944231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123412866-C-A

121944235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123412870-G-A

121948160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123415540-T-C

121948160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123415540-T-G

121948209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123415610-T-A

121948220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123415621-A-G

http://identifiers.org/hco/12/GRCh38#121948261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123415662-C-A

121948308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123415713-A-G

http://identifiers.org/hco/12/GRCh38#121948941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123416289-C-A

http://identifiers.org/hco/12/GRCh38#121948953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123416333-C-A

121948953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123416333-C-T

121948963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123416343-T-A

http://identifiers.org/hco/12/GRCh38#121949006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123416389-C-A

121949006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123416389-C-G

121949006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123416389-C-T

121949049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123416432-A-G

http://identifiers.org/hco/12/GRCh38#121949057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123416440-C-A

121949057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123416440-C-T

121949079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123416471-G-T

http://identifiers.org/hco/12/GRCh38#121949134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123416540-C-A

121949174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123416578-G-A

121949174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123416578-G-T

http://identifiers.org/hco/12/GRCh38#121949217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123416626-C-A

121949217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123416626-C-T

121951334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123417836-T-A

121951334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123417836-T-C

121951334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123417836-T-G

http://identifiers.org/hco/12/GRCh38#121951337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123417839-C-A

121951337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123417839-C-G

121951337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123417839-C-T

http://identifiers.org/hco/12/GRCh38#121951371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123417890-C-A

121951371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123417890-C-T

121951376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123417895-T-C

121951376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123417895-T-G

121951441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123417959-G-A

121951441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123417959-G-T

121951575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123418094-A-G

http://identifiers.org/hco/12/GRCh38#121951602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123418121-C-A

121951602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123418121-C-T

121951603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123418122-T-G

121951607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123418126-G-T

121953683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123420802-T-C

http://identifiers.org/hco/12/GRCh38#121953771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123420887-C-A

121953815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123420919-G-T

121953977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123421243-T-A

121953977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123421243-T-C

121953977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123421243-T-G

121953985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123421266-G-A

121953985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123421266-G-T

http://identifiers.org/hco/12/GRCh38#121954033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123421317-C-A

121954033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123421317-C-T

121954079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123421373-A-G

121954079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123421373-A-T

http://identifiers.org/hco/12/GRCh38#121954248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123421547-C-A

121954363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123421660-A-G

121955684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123423223-T-A

121955786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123423323-A-G

121956050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123423559-T-C

121956755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424067-C-G

121956943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424171-T-G

http://identifiers.org/hco/12/GRCh38#121956945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123424173-C-A

121956975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424195-A-T

121956978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424198-G-A

121956978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424198-G-T

121957001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424228-T-C

121957001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424228-T-G

http://identifiers.org/hco/12/GRCh38#121957012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123424240-A-C

121957012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424240-A-G

121957054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424282-G-T

121957205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123424433-C-T

121957299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424527-T-G

121957334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424562-A-G

http://identifiers.org/hco/12/GRCh38#121957337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123424565-C-A

121957337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424565-C-T

121957338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424566-A-G

121957345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424581-G-A

http://identifiers.org/hco/12/GRCh38#121957358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123424594-C-A

121957358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424594-C-G

121957506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424622-C-G

121957506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424622-C-T

121958116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123425068-G-A

121958200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123425152-T-C

http://identifiers.org/hco/12/GRCh38#121958800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123425567-C-A

121958800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123425567-C-G

121958800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123425567-C-T

121958879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123425612-A-T

121958920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123425654-C-G

121958920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123425654-C-T

http://identifiers.org/hco/12/GRCh38#121958968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123425702-A-C

121958968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123425702-A-G

121959046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123425780-T-A

121959046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123425780-T-C

121959116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123425843-C-T

http://identifiers.org/hco/12/GRCh38#121959239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123425964-C-A

http://identifiers.org/hco/12/GRCh38#121959434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123426230-C-A

121959434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123426230-C-T

http://identifiers.org/hco/12/GRCh38#121959460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123426265-C-A

121959460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123426265-C-G

121959460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123426265-C-T

http://identifiers.org/hco/12/GRCh38#121959479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123426276-C-A

121959479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123426276-C-G

121959479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123426276-C-T

http://identifiers.org/hco/12/GRCh38#121959565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123426357-C-A

121959565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123426357-C-G

121959565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123426357-C-T

http://identifiers.org/hco/12/GRCh38#121959592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123426379-C-A

121959592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123426379-C-T

http://identifiers.org/hco/12/GRCh38#121959603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123426390-C-A

121959690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123426430-A-G

121959806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123426532-G-T

121960685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense variant
orthologous variants: 123426806-G-A

121960797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123426921-T-C

121960842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123426985-G-A

121960842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123426985-G-T

121961036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123427197-C-T

121961043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123427204-T-C

121961369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123427466-C-T

121961374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123427471-A-G

121961395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123427492-T-G

121961442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123427514-G-A

121961451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123427523-C-T

121961533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123427590-A-G

121961944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123427918-G-A

http://identifiers.org/hco/12/GRCh38#121961958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123427930-C-A

http://identifiers.org/hco/12/GRCh38#121962054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123428021-A-C

121962054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123428021-A-G

121962109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123428076-T-A

121962109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123428076-T-G

121962168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123428135-C-T

121962203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123428152-A-T

121962221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123428170-T-A

121962221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123428170-T-C

121962288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123428235-G-A

121962288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123428235-G-T

121962314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123428261-G-A

121962314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123428261-G-T

121965026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123432384-G-T

http://identifiers.org/hco/12/GRCh38#121965066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#123432423-A-C

121965330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123432685-G-A

121965348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123432705-G-A

121965559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123432914-C-T

121966925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123435457-T-A

121966925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123435457-T-G

http://identifiers.org/hco/12/GRCh38#121966930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123435459-A-C

121966947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123435473-G-T

121967123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123435657-G-A

121967169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123435703-A-G

http://identifiers.org/hco/12/GRCh38#121967171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123435705-C-A

121967171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123435705-C-T

http://identifiers.org/hco/12/GRCh38#121967179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123435713-A-C

121967179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123435713-A-G

http://identifiers.org/hco/12/GRCh38#121967188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123435716-C-A

121967188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123435716-C-T

121967426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436001-G-A

121967441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436016-G-A

121967441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436016-G-C

121967444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436019-T-C

121967513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436059-T-C

http://identifiers.org/hco/12/GRCh38#121967526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123436072-C-A

121967532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436078-C-G

121967532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436078-C-T

121967562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436105-C-G

121967562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436105-C-T

121967563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436106-G-A

121967929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436465-G-A

121967929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436465-G-T

http://identifiers.org/hco/12/GRCh38#121967984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123436508-C-A

121967986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436510-A-G

121968032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123436556-C-T

121968149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123436673-G-A

121968173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436697-C-T

121968257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436941-A-G

121968257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436941-A-T

121968259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436943-G-A

121968280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436964-G-A

121968312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436996-T-C

http://identifiers.org/hco/12/GRCh38#121968381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123437045-C-A

121968381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123437045-C-T

121968544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123437201-C-T

121968582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123437241-G-A

121968597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123437256-G-C

121968774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123438009-A-T

http://identifiers.org/hco/12/GRCh38#121968831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123438069-C-A

121968831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123438069-C-T

121968987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123438179-G-A

121968987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123438179-G-C

http://identifiers.org/hco/12/GRCh38#121969004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123438196-C-A

121969004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123438196-C-T

121969031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123438212-A-G

121969335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123438504-G-C

121969774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123438665-G-A

121969915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123438755-A-G

http://identifiers.org/hco/12/GRCh38#121969960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123438801-C-A

121974383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123439631-T-C

121974863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123440089-G-A

121975280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: synonymous variant
orthologous variants: 123440473-C-T

121975616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: synonymous variant
orthologous variants: 123440831-A-G

121975752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123440961-A-G

121979893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123443009-C-T

121979912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123443028-A-G

121979925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123443041-C-T

121979972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123443086-C-T

121980035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123443152-G-A

121980183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123443298-C-T

121980187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123443302-T-C

121983792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123445095-G-C

121983826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123445129-A-G

121983899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123445196-A-G

121983909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123445208-A-G

121984240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123445518-C-T

121984697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123445735-C-G

http://identifiers.org/hco/12/GRCh38#121984798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123445795-C-A

121984878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123445869-T-C

121986880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123448317-C-G

121986940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123448395-G-A

121987047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123448500-T-C

121987062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123448515-C-T

121987446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123448805-G-T

http://identifiers.org/hco/12/GRCh38#121987972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123449226-A-C

121988025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123449272-C-T

121988327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123449516-C-T

121989644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123452139-T-G

121989661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123452151-C-G

121989661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123452151-C-T

121989818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123452364-C-T

121991299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123453461-C-G

121991763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123453757-G-A

121991942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123453832-G-A

121991942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123453832-G-C

121991942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123453832-G-T

121992115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123453982-A-T

121992166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123454027-T-G

121992221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123454082-T-C

121992355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123454205-T-C

121992373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123454254-C-T

121992413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123454340-T-C

121992458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123454384-G-A

121992537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, undefined
orthologous variants: 123454462-A-G

121992555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron variant
orthologous variants: 123454480-T-A

http://identifiers.org/hco/12/GRCh38#121999793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123460573-A-C

121999889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123460669-C-T

122000080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123460865-G-A

122000080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123460865-G-T

http://identifiers.org/hco/12/GRCh38#122001472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123462354-C-A

122001472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123462354-C-T

http://identifiers.org/hco/12/GRCh38#122001474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123462356-C-A

http://identifiers.org/hco/12/GRCh38#122001484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123462365-C-A

http://identifiers.org/hco/12/GRCh38#122001799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123462696-C-A

122001799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123462696-C-G

122001864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123462767-G-A

122001864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123462767-G-T

122003647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123464576-G-A

122003647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123464576-G-C

122003755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123464684-T-A

http://identifiers.org/hco/12/GRCh38#122003859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#123464794-C-A

122003859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123464794-C-T

122003860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123464795-T-C