http://identifiers.org/hco/11/GRCh38#10511699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110412770-C-A

http://identifiers.org/hco/11/GRCh38#10511915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110412965-C-A

10512007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110413057-C-T

10512024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110413073-T-C

10512086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110413131-G-A

10512172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110413223-G-T

10512952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110414379-A-G

http://identifiers.org/hco/11/GRCh38#10513057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110414469-C-A

http://identifiers.org/hco/11/GRCh38#10513083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110414491-A-C

10513083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110414491-A-G

10513109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110414507-G-A

10513109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110414507-G-T

10513141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110414538-T-C

http://identifiers.org/hco/11/GRCh38#10513153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110414551-C-A

http://identifiers.org/hco/11/GRCh38#10513188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110414582-C-A

10513201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110414595-A-G

10513215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110414614-A-G

http://identifiers.org/hco/11/GRCh38#10513249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110414657-C-A

10513336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110414767-A-G

10513352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110414783-A-G

10513352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110414783-A-T

10513380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110414813-A-T

10513542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110414973-T-C

10514143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415251-G-A

10514143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415251-G-C

10514288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415393-T-G

10514324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415414-G-A

10514389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415477-G-A

10514389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415477-G-T

http://identifiers.org/hco/11/GRCh38#10514561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110415594-A-C

10514561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415594-A-T

10514683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415687-G-T

10514773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415773-G-A

10514773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415773-G-C

10514773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415773-G-T

http://identifiers.org/hco/11/GRCh38#10514785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110415782-C-A

10514785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415782-C-G

10514785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415782-C-T

10514862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110415852-C-T

http://identifiers.org/hco/11/GRCh38#10515178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110416166-A-C

10515178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416166-A-G

10515179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416167-T-A

10515179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416167-T-C

10515179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416167-T-G

http://identifiers.org/hco/11/GRCh38#10515249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110416227-A-C

10515249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416227-A-G

10515325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416301-C-G

10515325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416301-C-T

10515347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416314-T-C

10515349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416316-T-G

http://identifiers.org/hco/11/GRCh38#10515356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110416323-C-A

10515356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416323-C-T

10515426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416435-A-G

10515471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416490-C-G

10515478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416495-T-C

http://identifiers.org/hco/11/GRCh38#10515583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110416593-C-A

10515597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416607-T-G

10515643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416653-G-A

10515643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416653-G-C

10515643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416653-G-T

10515752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110416851-T-C

10515960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417061-G-A

http://identifiers.org/hco/11/GRCh38#10516020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110417121-C-A

http://identifiers.org/hco/11/GRCh38#10516048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110417149-C-A

10516061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417160-T-G

10516062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417161-G-A

10516062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417161-G-T

10516367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417465-A-G

10516434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417521-A-G

10516522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417590-G-T

10516527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417595-C-T

10516586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417654-C-T

10516609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417671-G-A

10516609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417671-G-T

10516889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417894-A-G

10517008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110417973-T-C

10517084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110418050-A-G

10517085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110418051-T-C

10517085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110418051-T-G

10517149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110418108-G-A

10517575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110418362-G-A

10517614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110418405-G-C

10517614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110418405-G-T

10517650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110418443-A-G

10517651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110418444-G-T

10517660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110418453-A-G

10517661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110418454-G-A

10517661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110418454-G-T

10518209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110419711-C-T

10518356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110419829-A-G

http://identifiers.org/hco/11/GRCh38#10518369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110419845-C-A

10518433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110419905-G-A

http://identifiers.org/hco/11/GRCh38#10518453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110419925-C-A

10518489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110419966-A-G

10518493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110419970-G-T

10518512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110419992-A-G

http://identifiers.org/hco/11/GRCh38#10518581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110420067-C-A

10518581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110420067-C-G

10519078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: missense variant
orthologous variants: 110420505-G-C

10519291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110420716-T-C

10519410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110420833-T-C

10521101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110421071-T-G

http://identifiers.org/hco/11/GRCh38#10521138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110421103-C-A

10521138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110421103-C-T

10521298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110421234-T-C

http://identifiers.org/hco/11/GRCh38#10521596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110421453-A-C

10521596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110421453-A-T

10521638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110421494-A-G

10521841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110421708-G-T

10522237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110422234-G-A

http://identifiers.org/hco/11/GRCh38#10522245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110422242-C-A

10522445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110422419-T-G

10522915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110422732-G-A

10523184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110423018-T-C

10523231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110423062-C-G

10523388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110423146-T-C

10523488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110423201-G-T

10524635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110423953-G-T

10524640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110423958-T-C

10524950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110424247-A-G

10524972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110424269-G-A

10525142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110424392-T-A

10525152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110424402-T-A

10525174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110424406-T-C

10525178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110424410-T-C

10525185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 110424417-T-C

10525188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: intron variant
orthologous variants: 110424420-A-T

10525274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110424506-A-G

10525342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 110424574-G-A

10525482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110424673-T-G

10525555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110424742-G-T

10525590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110424778-C-T

10526879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110426675-C-T

10527112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110427767-T-C

10527112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110427767-T-G

10527167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110427816-T-G

10527855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110428563-G-A

10528577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110430406-T-C

10529167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110430874-G-C

10529599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110431265-C-T

10529666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110431331-G-C

10530061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110432002-A-G

10530385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110432355-T-C

10530385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110432355-T-G

10530497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110432445-G-A

10530497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110432445-G-T

10530904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110433188-T-C

10531060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110433316-A-G

10531135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110433366-G-A

10531765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110433827-G-A

10531765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110433827-G-T

http://identifiers.org/hco/11/GRCh38#10531789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110433834-C-A

10531839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110433888-A-G

10531862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110433912-C-T

10531913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110433960-G-T

10531927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110433974-G-A

10531927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110433974-G-T

10532770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110434797-G-T

10532771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110434798-G-A

10532941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110434945-C-T

10533270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110435490-C-G

10533776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110436053-C-T

10533780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110436059-G-C

10533882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110436159-A-G

10533882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110436159-A-T

10534003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110436271-G-A

10534197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110436469-A-G

10535257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110437658-C-G

10535344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110437800-G-A

10535420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110437875-T-A

10535425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110437880-G-A

10535508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110437952-T-A

10535508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110437952-T-C

10535508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110437952-T-G

10535593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110438105-C-T

10535732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110438357-A-G

10535744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110438369-G-C

10535779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110438397-G-C

10535986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110438759-A-G

10536166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110438949-G-C

10536301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110439065-C-T

10536526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110439298-C-G

10536907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110439537-G-T

10537010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110439640-A-G

10537034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110439665-A-G

10537108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110439751-T-C

10537400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110440180-G-A

10537495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110440263-T-C

10537506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110440275-A-G

10537764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110440469-C-T

10537801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110440502-T-A

10538281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110440863-A-G

10538868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441324-C-G

10538870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441326-C-G

10538892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441348-T-A

10538892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441348-T-C

10539044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441478-G-T

http://identifiers.org/hco/11/GRCh38#10539740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110442278-C-A

10539740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110442278-C-G

10539740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110442278-C-T

10539779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110442307-C-T

10540044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110442654-C-G

10540217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110442802-T-A

10540622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110443121-G-A

10540687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110443157-A-G

10540720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110443192-G-T

10540723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110443195-T-C

10540748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110443219-C-T

10540826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110443284-G-C

10540826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110443284-G-T

10540920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110443352-A-G

http://identifiers.org/hco/11/GRCh38#10540954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110443377-C-A

10540954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110443377-C-G

10540954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110443377-C-T

10540985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110443421-G-A

10540985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110443421-G-T

10541061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110443484-G-T

http://identifiers.org/hco/11/GRCh38#10541138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#110443560-C-A

10541138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110443560-C-T

10541165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110443584-G-A

10541165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21159
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110443584-G-T