10033607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129369887-T-G

10033608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129369888-G-A

http://identifiers.org/hco/12/GRCh38#10033647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129369959-C-A

10033658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129369970-A-G

10033684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129369994-A-G

10033845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129370157-G-A

10033868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129370173-A-G

10033887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129370178-A-T

10033963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129370256-A-T

10034002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129370295-G-C

10036318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129370699-A-G

10036472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129371069-G-T

10036565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129371187-T-A

http://identifiers.org/hco/12/GRCh38#10037885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129371685-C-A

10038442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129373263-T-C

http://identifiers.org/hco/12/GRCh38#10038455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129373299-A-C

10038536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129373397-T-A

10038625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129373513-A-T

10038738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129373620-G-A

10039084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129376987-C-T

10039231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129377130-C-T

10039268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129377169-A-G

10039649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129377555-A-G

10039694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129377603-C-T

10040180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378115-T-G

10040209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378144-T-C

10040293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378235-A-G

10040344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378262-C-T

10040771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378357-G-T

10040780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378366-A-G

10040783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378369-A-G

10040790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378376-T-C

10040820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378406-A-G

http://identifiers.org/hco/12/GRCh38#10040852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129378439-C-A

10040852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129378439-C-G

10040852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129378439-C-T

10040875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129378462-T-A

10040875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129378462-T-C

10040923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129378510-T-A

10040923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129378510-T-C

http://identifiers.org/hco/12/GRCh38#10041324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129378576-C-A

10041324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378576-C-T

10041340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378592-A-G

10041340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378592-A-T

http://identifiers.org/hco/12/GRCh38#10041344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129378596-C-A

10041344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378596-C-T

10041361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378610-T-A

10041361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378610-T-C

10041557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 129378793-G-A

10041587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 129378823-T-C

10041650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378886-G-T

10041651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378887-A-G

10041653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378889-G-A

10041653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378889-G-C

10041653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129378889-G-T

10041841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129379066-T-G

10041940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129379164-C-T

10042108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129379330-G-A

10042151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129379405-A-T

10042427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129379698-G-A

10042443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129379715-A-G

10042687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380022-A-T

10042722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380057-C-G

10042893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380208-C-T

http://identifiers.org/hco/12/GRCh38#10043021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129380339-A-C

10043099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380422-A-G

10043157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380468-T-A

10043157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380468-T-C

10043157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380468-T-G

10043161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380472-T-C

10043168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380479-A-G

10043171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380482-T-C

http://identifiers.org/hco/12/GRCh38#10043188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129380497-C-A

10043188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380497-C-T

10043268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129380577-G-A

10043270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129380579-A-G

10043312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129380622-A-G

10043318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129380628-T-C

http://identifiers.org/hco/12/GRCh38#10043330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129380641-C-A

10043330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380641-C-G

10043330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129380641-C-T

10045176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129381779-G-A

10045217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129381817-C-T

10045243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129381843-C-T

10045278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129381878-T-C

10045296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129381896-C-T

10045373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129381970-A-T

10045418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129382008-A-G

10045466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129382051-C-T

http://identifiers.org/hco/12/GRCh38#10045540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129382125-C-A

10045540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129382125-C-G

10045540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129382125-C-T

10045587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129382172-T-A

10045587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129382172-T-C

10045643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129382228-G-A

10045643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129382228-G-T

http://identifiers.org/hco/12/GRCh38#10045644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129382229-C-A

10045644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129382229-C-G

10045644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129382229-C-T

10045690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129382274-T-A

10045690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129382274-T-C

10045700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129382284-A-G

10045775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129382333-C-T

10045783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129382341-C-T

http://identifiers.org/hco/12/GRCh38#10045800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129382358-C-A

10045911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129382452-A-T

10045959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129382490-G-C

10046268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129382775-T-C

10046641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129383209-G-A

10046732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129383296-T-A

10046989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129383544-G-A

10046989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129383544-G-C

10047212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129383778-T-C

10047250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129383815-A-T

10047470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129384038-C-T

10050541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129384202-A-G

10050541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129384202-A-T

10050745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129384401-C-G

10050858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129384510-G-T

10050892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129384528-C-T

10051649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129384980-C-G

10051649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129384980-C-T

10051766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129385083-T-C

10051803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129385132-A-T

10051842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129385169-C-T

10051905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129385214-G-T

10052053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 129385353-G-T

10052306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129385578-G-T

10052340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129385613-A-G

10052344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129385617-G-A

10052344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129385617-G-T

http://identifiers.org/hco/12/GRCh38#10052407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129385651-A-C

10052407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129385651-A-G

10052453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129385698-A-T

10052475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129385719-T-G

10052524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129385766-G-T

http://identifiers.org/hco/12/GRCh38#10052530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129385772-A-C

10052563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129385795-T-A

10052563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129385795-T-C

http://identifiers.org/hco/12/GRCh38#10052571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129385800-C-A

10052571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129385800-C-T

10052586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129385815-G-T

10052695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129385925-A-G

http://identifiers.org/hco/12/GRCh38#10052808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129386038-C-A

10052808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129386038-C-G

10052808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129386038-C-T

10052822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129386043-T-G

10053087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129386255-C-T

10053931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129386914-A-T

10053978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129386979-T-C

http://identifiers.org/hco/12/GRCh38#10054169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129387155-C-A

10054169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129387155-C-T

http://identifiers.org/hco/12/GRCh38#10054207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129387181-C-A

10054207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129387181-C-T

10054209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129387183-T-C

http://identifiers.org/hco/12/GRCh38#10054214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129387188-C-A

http://identifiers.org/hco/12/GRCh38#10054230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129387199-C-A

10054379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129387373-A-G

10054380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129387374-T-A

http://identifiers.org/hco/12/GRCh38#10054401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129387394-C-A

10054401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129387394-C-G

10054401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129387394-C-T

10054423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129387415-G-C

10054423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129387415-G-T

10058088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129388084-G-A

10058349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129388376-G-A

http://identifiers.org/hco/12/GRCh38#10060739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129391806-C-A

http://identifiers.org/hco/12/GRCh38#10060788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129391856-A-C

10060845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129391880-A-T

10060903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129391944-T-C

10060903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129391944-T-G

10060931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129391977-G-A

10060931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129391977-G-C

10060931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129391977-G-T

http://identifiers.org/hco/12/GRCh38#10060949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129391995-C-A

10060949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129391995-C-T

http://identifiers.org/hco/12/GRCh38#10060973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129392038-C-A

http://identifiers.org/hco/12/GRCh38#10061013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129392076-C-A

http://identifiers.org/hco/12/GRCh38#10061046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129392102-A-C

10061046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129392102-A-G

10061061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129392126-G-A

10061061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129392126-G-T

10061110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129392168-A-T

http://identifiers.org/hco/12/GRCh38#10061410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129394235-C-A

10061410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129394235-C-G

10061410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129394235-C-T

10061463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129394288-C-G

10061516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129394341-T-G

10061635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129394448-G-A

http://identifiers.org/hco/12/GRCh38#10062166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129395272-A-C

10062356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129395456-G-A

10062365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129395465-C-T

10062608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129395690-T-C

http://identifiers.org/hco/12/GRCh38#10062911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129396338-C-A

10062920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129396346-G-T

http://identifiers.org/hco/12/GRCh38#10062930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129396356-C-A

10062943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129396369-A-G

10062992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129396381-G-T

10063001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129396390-T-C

10063001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129396390-T-G

10063013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129396402-A-G

10063021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129396410-A-G

10063124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129396514-T-C

10063220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129396610-T-A

10063246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129396636-T-A

10063246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129396636-T-C

10063284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129396674-G-A

10063445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129396832-T-C

10064212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129397350-A-G

10064394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129397521-G-A

10064695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129397965-G-A

10064695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129397965-G-T

10064713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129397988-T-C

10064750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: synonymous variant
orthologous variants: 129398022-T-C

http://identifiers.org/hco/12/GRCh38#10064940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129398208-C-A

10064987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129398256-A-G

http://identifiers.org/hco/12/GRCh38#10064995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129398264-C-A

10065165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129398857-T-C

10065206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129398896-T-C

http://identifiers.org/hco/12/GRCh38#10065425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129399109-C-A

10065425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129399109-C-G

10065425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: intron variant
orthologous variants: 129399109-C-T

10065507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: missense variant
orthologous variants: 129399196-G-C

10065512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: missense variant
orthologous variants: 129399201-G-T

10065545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: synonymous variant
orthologous variants: 129399234-C-T

10065591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: missense variant
orthologous variants: 129399280-T-C

10065644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 3 prime UTR variant
orthologous variants: 129399331-T-A

10065719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 3 prime UTR variant
orthologous variants: 129399381-G-A

10065719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 3 prime UTR variant
orthologous variants: 129399381-G-T

10065761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 3 prime UTR variant
orthologous variants: 129399419-G-A

10065761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 3 prime UTR variant
orthologous variants: 129399419-G-T

10065794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 3 prime UTR variant
orthologous variants: 129399452-A-T

http://identifiers.org/hco/12/GRCh38#10065853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#129399512-C-A

10065853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 3 prime UTR variant
orthologous variants: 129399512-C-T

10065906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 3 prime UTR variant
orthologous variants: 129399562-T-C

10065906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 3 prime UTR variant
orthologous variants: 129399562-T-G

10065914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 3 prime UTR variant
orthologous variants: 129399570-G-T

10065976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26705
most severe consequence: 3 prime UTR variant
orthologous variants: 129399628-G-T