http://identifiers.org/hco/10/GRCh38#67922142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63154004-C-A

67922417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3 prime UTR variant
orthologous variants: 63153717-G-A

67922417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3 prime UTR variant
orthologous variants: 63153717-G-T

67922556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 63153591-A-G

67922557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 63153590-T-C

67922569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 63153577-G-C

67922569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 63153577-G-T

67922763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 63153402-G-C

67922763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 63153402-G-T

67922818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 63153356-C-T

67932506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63151712-G-A

67932506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63151712-G-T

67932552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63151670-A-G

http://identifiers.org/hco/10/GRCh38#67932562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63151653-C-A

67932562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63151653-C-T

http://identifiers.org/hco/10/GRCh38#67932796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63151418-C-A

67935884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63150707-C-T

67935963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63150640-T-C

67936121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63150377-T-C

67936195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 63150304-A-G

67940895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63147447-A-G

67940930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63147419-C-T

67940978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 63147371-G-C

67941122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63147224-A-G

http://identifiers.org/hco/10/GRCh38#67941180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63147172-C-A

67941180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63147172-C-G

67941238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63147100-T-G

67953161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63145405-T-G

67953309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63145248-C-T

67954075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63144669-G-T

67954216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63144530-T-C

67954254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63144496-A-G

http://identifiers.org/hco/10/GRCh38#67954257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63144493-C-A

67954257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63144493-C-T

67954259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63144491-A-G

67954261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63144489-G-A

67954261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63144489-G-C

67954261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63144489-G-T

67954326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63144425-C-G

67954326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63144425-C-T

http://identifiers.org/hco/10/GRCh38#67954760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63144062-A-C

67956486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63142664-T-C

http://identifiers.org/hco/10/GRCh38#67956574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63142574-C-A

67956574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63142574-C-T

67956734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63142417-T-C

http://identifiers.org/hco/10/GRCh38#67956765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63142389-C-A

67956765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63142389-C-T

67956778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63142353-T-C

http://identifiers.org/hco/10/GRCh38#67956781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63142350-A-C

67956781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63142350-A-T

67956801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63142330-G-T

http://identifiers.org/hco/10/GRCh38#67956841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63142272-C-A

67957080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63142046-T-C

67957080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63142046-T-G

67958506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63140376-T-C

67958575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63140313-T-C

http://identifiers.org/hco/10/GRCh38#67958968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63139807-C-A

67958984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63139791-G-T

67959004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63139754-T-C

67959058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63139693-G-A

67959058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63139693-G-T

67959068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63139685-G-A

67959068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63139685-G-C

67959068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63139685-G-T

67959069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63139684-A-G

67959154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63139604-A-G

67959214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63139556-G-A

67959214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63139556-G-T

http://identifiers.org/hco/10/GRCh38#67959289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63139483-C-A

67959925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63138137-C-G

67960024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63138059-G-A

67966335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63135304-C-T

67966640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63135059-C-T

67975782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63132182-A-G

http://identifiers.org/hco/10/GRCh38#67985462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63130843-A-C

67985613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63130718-A-G

67985883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63130483-T-C

67986083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63130073-C-T

67986661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63129384-T-C

67986689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63129356-G-A

67986729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63129324-T-A

67986746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63129309-G-A

67987385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63127664-A-G

67987511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63127532-G-A

67987886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63127203-T-C

67987960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63127143-G-T

http://identifiers.org/hco/10/GRCh38#67988257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63126840-C-A

67988257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63126840-C-T

67988350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63126752-A-G

http://identifiers.org/hco/10/GRCh38#67988495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63126618-C-A

67988495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63126618-C-T

67988997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63126126-T-C

67989032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63126085-C-T

http://identifiers.org/hco/10/GRCh38#67990097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63125152-C-A

67990097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63125152-C-T

67990140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63125114-G-A

67990140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63125114-G-T

http://identifiers.org/hco/10/GRCh38#67990152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63125079-A-C

http://identifiers.org/hco/10/GRCh38#67990819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63123873-A-C

67990819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63123873-A-G

67990866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63123825-A-G

http://identifiers.org/hco/10/GRCh38#67990876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63123816-C-A

67990876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63123816-C-T

67991029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63123662-A-G

67991029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63123662-A-T

67991092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63123407-A-G

67991128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63123367-A-G

http://identifiers.org/hco/10/GRCh38#67991142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63123353-A-C

67991142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 63123353-A-G

http://identifiers.org/hco/10/GRCh38#67992055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63120752-C-A

67992055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63120752-C-G

67992055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63120752-C-T

http://identifiers.org/hco/10/GRCh38#67992059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63120756-C-A

67992087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63120812-G-A

67992087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63120812-G-T

67992289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 63121828-T-C

67992393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63121715-A-G

67992393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63121715-A-T

http://identifiers.org/hco/10/GRCh38#67992427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63121681-C-A

67992482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63121623-T-C

http://identifiers.org/hco/10/GRCh38#67992504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63121599-A-C

http://identifiers.org/hco/10/GRCh38#67992508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63121595-C-A

67992508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63121595-C-T

67992812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63121314-A-G

http://identifiers.org/hco/10/GRCh38#67992833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63121290-C-A

67992833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63121290-C-T

67992835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63121288-G-T

67992843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63121282-G-A

http://identifiers.org/hco/10/GRCh38#67992878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63121249-C-A

67992967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120965-T-A

67992967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120965-T-C

67993023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120917-G-C

67993023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120917-G-T

http://identifiers.org/hco/10/GRCh38#67993024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63120916-A-C

67993024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120916-A-T

http://identifiers.org/hco/10/GRCh38#67993200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63120756-C-A

67993200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120756-C-T

67993204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120752-G-A

67993204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120752-G-T

http://identifiers.org/hco/10/GRCh38#67993235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63120722-C-A

67993252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120705-G-A

67993252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120705-G-T

67993281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120691-G-A

67993281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120691-G-T

67993321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120647-G-A

67993981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120399-T-C

67994035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120335-T-A

67994035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63120335-T-C

68013990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63119154-A-G

68014002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63119142-A-G

http://identifiers.org/hco/10/GRCh38#68014240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63118904-C-A

68014240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63118904-C-T

68025498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63114290-A-G

68025770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63114015-C-T

68032181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63111763-G-C

68032181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63111763-G-T

68032185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63111759-A-T

http://identifiers.org/hco/10/GRCh38#68032220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63111654-A-C

http://identifiers.org/hco/10/GRCh38#68032681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63110952-C-A

68032681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63110952-C-T

68032741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63110898-G-T

68032954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63110702-A-G

68032954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63110702-A-T

68033079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63110592-T-G

68033477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63110239-A-T

68033753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63109854-T-C

68033949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63109465-C-T

68033976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63109438-T-C

http://identifiers.org/hco/10/GRCh38#68034371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63109081-A-C

68035014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63108512-A-G

68038018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63105539-G-A

68038018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63105539-G-T

68038177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 63105397-A-G

http://identifiers.org/hco/10/GRCh38#68038233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63105344-A-C

68038233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63105344-A-G

68038245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63105326-T-C

68038288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63105286-T-C

http://identifiers.org/hco/10/GRCh38#68038289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63105285-C-A

http://identifiers.org/hco/10/GRCh38#68038293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63105281-C-A

68038293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63105281-C-G

http://identifiers.org/hco/10/GRCh38#68038297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63105277-C-A

68038297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63105277-C-T

68038421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63105172-A-G

68038528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63105074-T-A

68038608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63105037-C-T

68039362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63104758-T-A

68039362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63104758-T-C

68039362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63104758-T-G

68039489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_acceptor_variant
orthologous variants: 63104632-C-T

68039508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63104613-G-T

68039569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63104551-G-T

68039571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63104549-G-A

68039765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63104369-C-T

68039785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63104353-C-T

68039798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 63104340-T-C

68040044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63104134-C-T

68044289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63100069-G-A

68044289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63100069-G-T

68044766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63099461-T-G

http://identifiers.org/hco/10/GRCh38#68045193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63099029-C-A

68045195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63099027-C-T

68045197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63099025-C-T

68045468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63098818-G-A

68045513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63098763-A-G

68045925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63098139-T-C

68056986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63093697-G-T

68059407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63091879-T-C

http://identifiers.org/hco/10/GRCh38#68060731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63091270-A-C

68060843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63090984-T-C

68062112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63090048-G-A

68062352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63089847-T-G

68062356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63089843-T-A

http://identifiers.org/hco/10/GRCh38#68065493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63087595-A-C

68066552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63086436-G-T

68066803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63086168-T-C

http://identifiers.org/hco/10/GRCh38#68066903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63086041-C-A

68066903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 63086041-C-T

http://identifiers.org/hco/10/GRCh38#68066963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63085984-C-A

68067710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63085276-T-C

http://identifiers.org/hco/10/GRCh38#68067724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63085256-C-A

68068991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63085183-G-A

68068991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63085183-G-T

68069145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63085072-A-G

68069152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63085065-G-C

68069154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63085063-T-C

68069209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63085016-A-G

68069381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63084836-T-C

68069406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63084702-A-G

68069408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63084700-G-A

68069408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63084700-G-C

68069408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63084700-G-T

68069435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63084673-G-T

68069459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63084649-T-C

68069495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63084615-T-C

68069571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63084546-G-A

68070121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63084219-A-G

68070203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63084133-A-G

68070621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63083868-A-G

68070806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63083812-C-G

68070806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63083812-C-T

http://identifiers.org/hco/10/GRCh38#68070872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63083757-A-C

http://identifiers.org/hco/10/GRCh38#68071243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63083415-A-C

68071285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63083388-C-T

68071767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63083124-T-C

68071843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63083036-C-G

68072024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63082815-T-A

68072067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63082761-C-T

68072083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63082748-T-A

68072104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63082735-T-C

68072105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63082734-C-T

68072383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63082462-T-C

68072409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63082436-A-G

68073029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63081756-T-G

68073263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63081531-A-G

68073270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63081524-G-A

http://identifiers.org/hco/10/GRCh38#68073532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63081333-C-A

http://identifiers.org/hco/10/GRCh38#68073570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#63081295-A-C

68074267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63080581-G-A

68074267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63080581-G-T

68074315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63080527-T-C

68074663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 63080162-C-T

68074711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63080135-G-A

68074711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63080135-G-C

68074711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63080135-G-T

68074841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63080028-C-T

68074888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63079989-G-T

68074932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63079954-G-A

68074932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63079954-G-C

68074932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63079954-G-T

68074986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63079901-G-A

68074986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63079901-G-C

68075000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63079887-G-T

68075090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63079814-G-A

68075108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63079795-C-T

68075234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 63079664-G-A

68075234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24521
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 63079664-G-T